Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables:
Gespeichert in:
Format: | Buch |
---|---|
Sprache: | English |
Veröffentlicht: |
Berlin [u.a.]
Springer
1993
|
Schlagworte: | |
Beschreibung: | Literaturangaben |
Beschreibung: | XIV, 182 S. Ill., graph. Darst. |
ISBN: | 3540567747 0387567747 |
Internformat
MARC
LEADER | 00000nam a2200000 c 4500 | ||
---|---|---|---|
001 | BV008100363 | ||
003 | DE-604 | ||
005 | 20160512 | ||
007 | t | ||
008 | 930712s1993 gw ad|| |||| 10||| eng d | ||
020 | |a 3540567747 |9 3-540-56774-7 | ||
020 | |a 0387567747 |9 0-387-56774-7 | ||
035 | |a (OCoLC)28550429 | ||
035 | |a (DE-599)BVBBV008100363 | ||
040 | |a DE-604 |b ger |e rakddb | ||
041 | 0 | |a eng | |
044 | |a gw |c DE | ||
049 | |a DE-355 |a DE-19 |a DE-12 |a DE-188 | ||
050 | 0 | |a RC632.P87 | |
082 | 0 | |a 616.3/9 |2 20 | |
084 | |a YC 7619 |0 (DE-625)153257:12925 |2 rvk | ||
245 | 1 | 0 | |a Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables |c U. Gresser (ed.). With contributions by R. A. de Abreu ... |
264 | 1 | |a Berlin [u.a.] |b Springer |c 1993 | |
300 | |a XIV, 182 S. |b Ill., graph. Darst. | ||
336 | |b txt |2 rdacontent | ||
337 | |b n |2 rdamedia | ||
338 | |b nc |2 rdacarrier | ||
500 | |a Literaturangaben | ||
650 | 4 | |a Enzymes |x deficiency | |
650 | 4 | |a Purine-Pyrimidine Metabolism, Inborn Errors |x genetics | |
650 | 4 | |a Purine-Pyrimidine Metabolism, Inborn Errors |x metabolism | |
650 | 4 | |a Purine-Pyrimidine Metabolism, Inborn Errors |x physiopathology | |
650 | 4 | |a Purines |x Metabolism |x Disorders | |
650 | 4 | |a Pyrimidines |x Metabolism |x Disorders | |
650 | 0 | 7 | |a Molekulargenetik |0 (DE-588)4039987-4 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Stoffwechselkrankheit |0 (DE-588)4057700-4 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Pyrimidinstoffwechselstörung |0 (DE-588)4321807-6 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Purinstoffwechsel |0 (DE-588)4176403-1 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Angeborene Krankheit |0 (DE-588)4331107-6 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Erbkrankheit |0 (DE-588)4015106-2 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Pyrimidinstoffwechsel |0 (DE-588)4195173-6 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Purinstoffwechselstörung |0 (DE-588)4205704-8 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Physiologische Chemie |0 (DE-588)4076124-1 |2 gnd |9 rswk-swf |
655 | 7 | |0 (DE-588)1071861417 |a Konferenzschrift |y 1991 |z München |2 gnd-content | |
689 | 0 | 0 | |a Purinstoffwechsel |0 (DE-588)4176403-1 |D s |
689 | 0 | 1 | |a Stoffwechselkrankheit |0 (DE-588)4057700-4 |D s |
689 | 0 | 2 | |a Angeborene Krankheit |0 (DE-588)4331107-6 |D s |
689 | 0 | |5 DE-604 | |
689 | 1 | 0 | |a Pyrimidinstoffwechsel |0 (DE-588)4195173-6 |D s |
689 | 1 | 1 | |a Stoffwechselkrankheit |0 (DE-588)4057700-4 |D s |
689 | 1 | 2 | |a Angeborene Krankheit |0 (DE-588)4331107-6 |D s |
689 | 1 | |5 DE-604 | |
689 | 2 | 0 | |a Purinstoffwechselstörung |0 (DE-588)4205704-8 |D s |
689 | 2 | 1 | |a Erbkrankheit |0 (DE-588)4015106-2 |D s |
689 | 2 | 2 | |a Molekulargenetik |0 (DE-588)4039987-4 |D s |
689 | 2 | |5 DE-604 | |
689 | 3 | 0 | |a Purinstoffwechselstörung |0 (DE-588)4205704-8 |D s |
689 | 3 | 1 | |a Erbkrankheit |0 (DE-588)4015106-2 |D s |
689 | 3 | 2 | |a Physiologische Chemie |0 (DE-588)4076124-1 |D s |
689 | 3 | |5 DE-604 | |
689 | 4 | 0 | |a Pyrimidinstoffwechselstörung |0 (DE-588)4321807-6 |D s |
689 | 4 | 1 | |a Erbkrankheit |0 (DE-588)4015106-2 |D s |
689 | 4 | 2 | |a Molekulargenetik |0 (DE-588)4039987-4 |D s |
689 | 4 | |5 DE-604 | |
689 | 5 | 0 | |a Pyrimidinstoffwechselstörung |0 (DE-588)4321807-6 |D s |
689 | 5 | 1 | |a Erbkrankheit |0 (DE-588)4015106-2 |D s |
689 | 5 | 2 | |a Physiologische Chemie |0 (DE-588)4076124-1 |D s |
689 | 5 | |5 DE-604 | |
700 | 1 | |a Gresser, Ursula |e Sonstige |0 (DE-588)172105293 |4 oth | |
700 | 1 | |a Abreu, R. A. de |e Sonstige |4 oth | |
999 | |a oai:aleph.bib-bvb.de:BVB01-005336337 |
Datensatz im Suchindex
_version_ | 1804122473489235968 |
---|---|
any_adam_object | |
author_GND | (DE-588)172105293 |
building | Verbundindex |
bvnumber | BV008100363 |
callnumber-first | R - Medicine |
callnumber-label | RC632 |
callnumber-raw | RC632.P87 |
callnumber-search | RC632.P87 |
callnumber-sort | RC 3632 P87 |
callnumber-subject | RC - Internal Medicine |
classification_rvk | YC 7619 |
ctrlnum | (OCoLC)28550429 (DE-599)BVBBV008100363 |
dewey-full | 616.3/9 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 616 - Diseases |
dewey-raw | 616.3/9 |
dewey-search | 616.3/9 |
dewey-sort | 3616.3 19 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
format | Book |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>03406nam a2200817 c 4500</leader><controlfield tag="001">BV008100363</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20160512 </controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">930712s1993 gw ad|| |||| 10||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">3540567747</subfield><subfield code="9">3-540-56774-7</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0387567747</subfield><subfield code="9">0-387-56774-7</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)28550429</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV008100363</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakddb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">DE</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-355</subfield><subfield code="a">DE-19</subfield><subfield code="a">DE-12</subfield><subfield code="a">DE-188</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RC632.P87</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">616.3/9</subfield><subfield code="2">20</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">YC 7619</subfield><subfield code="0">(DE-625)153257:12925</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables</subfield><subfield code="c">U. Gresser (ed.). With contributions by R. A. de Abreu ...</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Berlin [u.a.]</subfield><subfield code="b">Springer</subfield><subfield code="c">1993</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XIV, 182 S.</subfield><subfield code="b">Ill., graph. Darst.</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Literaturangaben</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Enzymes</subfield><subfield code="x">deficiency</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Purine-Pyrimidine Metabolism, Inborn Errors</subfield><subfield code="x">genetics</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Purine-Pyrimidine Metabolism, Inborn Errors</subfield><subfield code="x">metabolism</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Purine-Pyrimidine Metabolism, Inborn Errors</subfield><subfield code="x">physiopathology</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Purines</subfield><subfield code="x">Metabolism</subfield><subfield code="x">Disorders</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Pyrimidines</subfield><subfield code="x">Metabolism</subfield><subfield code="x">Disorders</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Molekulargenetik</subfield><subfield code="0">(DE-588)4039987-4</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Stoffwechselkrankheit</subfield><subfield code="0">(DE-588)4057700-4</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Pyrimidinstoffwechselstörung</subfield><subfield code="0">(DE-588)4321807-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Purinstoffwechsel</subfield><subfield code="0">(DE-588)4176403-1</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Angeborene Krankheit</subfield><subfield code="0">(DE-588)4331107-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Erbkrankheit</subfield><subfield code="0">(DE-588)4015106-2</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Pyrimidinstoffwechsel</subfield><subfield code="0">(DE-588)4195173-6</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Purinstoffwechselstörung</subfield><subfield code="0">(DE-588)4205704-8</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Physiologische Chemie</subfield><subfield code="0">(DE-588)4076124-1</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)1071861417</subfield><subfield code="a">Konferenzschrift</subfield><subfield code="y">1991</subfield><subfield code="z">München</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Purinstoffwechsel</subfield><subfield code="0">(DE-588)4176403-1</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Stoffwechselkrankheit</subfield><subfield code="0">(DE-588)4057700-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="2"><subfield code="a">Angeborene Krankheit</subfield><subfield code="0">(DE-588)4331107-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" ind2="0"><subfield code="a">Pyrimidinstoffwechsel</subfield><subfield code="0">(DE-588)4195173-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="1"><subfield code="a">Stoffwechselkrankheit</subfield><subfield code="0">(DE-588)4057700-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="2"><subfield code="a">Angeborene Krankheit</subfield><subfield code="0">(DE-588)4331107-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="2" ind2="0"><subfield code="a">Purinstoffwechselstörung</subfield><subfield code="0">(DE-588)4205704-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="2" ind2="1"><subfield code="a">Erbkrankheit</subfield><subfield code="0">(DE-588)4015106-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="2" ind2="2"><subfield code="a">Molekulargenetik</subfield><subfield code="0">(DE-588)4039987-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="2" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="3" ind2="0"><subfield code="a">Purinstoffwechselstörung</subfield><subfield code="0">(DE-588)4205704-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="3" ind2="1"><subfield code="a">Erbkrankheit</subfield><subfield code="0">(DE-588)4015106-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="3" ind2="2"><subfield code="a">Physiologische Chemie</subfield><subfield code="0">(DE-588)4076124-1</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="3" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="4" ind2="0"><subfield code="a">Pyrimidinstoffwechselstörung</subfield><subfield code="0">(DE-588)4321807-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="4" ind2="1"><subfield code="a">Erbkrankheit</subfield><subfield code="0">(DE-588)4015106-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="4" ind2="2"><subfield code="a">Molekulargenetik</subfield><subfield code="0">(DE-588)4039987-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="4" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="5" ind2="0"><subfield code="a">Pyrimidinstoffwechselstörung</subfield><subfield code="0">(DE-588)4321807-6</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="5" ind2="1"><subfield code="a">Erbkrankheit</subfield><subfield code="0">(DE-588)4015106-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="5" ind2="2"><subfield code="a">Physiologische Chemie</subfield><subfield code="0">(DE-588)4076124-1</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="5" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gresser, Ursula</subfield><subfield code="e">Sonstige</subfield><subfield code="0">(DE-588)172105293</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Abreu, R. A. de</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-005336337</subfield></datafield></record></collection> |
genre | (DE-588)1071861417 Konferenzschrift 1991 München gnd-content |
genre_facet | Konferenzschrift 1991 München |
id | DE-604.BV008100363 |
illustrated | Illustrated |
indexdate | 2024-07-09T17:14:26Z |
institution | BVB |
isbn | 3540567747 0387567747 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-005336337 |
oclc_num | 28550429 |
open_access_boolean | |
owner | DE-355 DE-BY-UBR DE-19 DE-BY-UBM DE-12 DE-188 |
owner_facet | DE-355 DE-BY-UBR DE-19 DE-BY-UBM DE-12 DE-188 |
physical | XIV, 182 S. Ill., graph. Darst. |
publishDate | 1993 |
publishDateSearch | 1993 |
publishDateSort | 1993 |
publisher | Springer |
record_format | marc |
spelling | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables U. Gresser (ed.). With contributions by R. A. de Abreu ... Berlin [u.a.] Springer 1993 XIV, 182 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Literaturangaben Enzymes deficiency Purine-Pyrimidine Metabolism, Inborn Errors genetics Purine-Pyrimidine Metabolism, Inborn Errors metabolism Purine-Pyrimidine Metabolism, Inborn Errors physiopathology Purines Metabolism Disorders Pyrimidines Metabolism Disorders Molekulargenetik (DE-588)4039987-4 gnd rswk-swf Stoffwechselkrankheit (DE-588)4057700-4 gnd rswk-swf Pyrimidinstoffwechselstörung (DE-588)4321807-6 gnd rswk-swf Purinstoffwechsel (DE-588)4176403-1 gnd rswk-swf Angeborene Krankheit (DE-588)4331107-6 gnd rswk-swf Erbkrankheit (DE-588)4015106-2 gnd rswk-swf Pyrimidinstoffwechsel (DE-588)4195173-6 gnd rswk-swf Purinstoffwechselstörung (DE-588)4205704-8 gnd rswk-swf Physiologische Chemie (DE-588)4076124-1 gnd rswk-swf (DE-588)1071861417 Konferenzschrift 1991 München gnd-content Purinstoffwechsel (DE-588)4176403-1 s Stoffwechselkrankheit (DE-588)4057700-4 s Angeborene Krankheit (DE-588)4331107-6 s DE-604 Pyrimidinstoffwechsel (DE-588)4195173-6 s Purinstoffwechselstörung (DE-588)4205704-8 s Erbkrankheit (DE-588)4015106-2 s Molekulargenetik (DE-588)4039987-4 s Physiologische Chemie (DE-588)4076124-1 s Pyrimidinstoffwechselstörung (DE-588)4321807-6 s Gresser, Ursula Sonstige (DE-588)172105293 oth Abreu, R. A. de Sonstige oth |
spellingShingle | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables Enzymes deficiency Purine-Pyrimidine Metabolism, Inborn Errors genetics Purine-Pyrimidine Metabolism, Inborn Errors metabolism Purine-Pyrimidine Metabolism, Inborn Errors physiopathology Purines Metabolism Disorders Pyrimidines Metabolism Disorders Molekulargenetik (DE-588)4039987-4 gnd Stoffwechselkrankheit (DE-588)4057700-4 gnd Pyrimidinstoffwechselstörung (DE-588)4321807-6 gnd Purinstoffwechsel (DE-588)4176403-1 gnd Angeborene Krankheit (DE-588)4331107-6 gnd Erbkrankheit (DE-588)4015106-2 gnd Pyrimidinstoffwechsel (DE-588)4195173-6 gnd Purinstoffwechselstörung (DE-588)4205704-8 gnd Physiologische Chemie (DE-588)4076124-1 gnd |
subject_GND | (DE-588)4039987-4 (DE-588)4057700-4 (DE-588)4321807-6 (DE-588)4176403-1 (DE-588)4331107-6 (DE-588)4015106-2 (DE-588)4195173-6 (DE-588)4205704-8 (DE-588)4076124-1 (DE-588)1071861417 |
title | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables |
title_auth | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables |
title_exact_search | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables |
title_full | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables U. Gresser (ed.). With contributions by R. A. de Abreu ... |
title_fullStr | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables U. Gresser (ed.). With contributions by R. A. de Abreu ... |
title_full_unstemmed | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables U. Gresser (ed.). With contributions by R. A. de Abreu ... |
title_short | Molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism ; with 41 tables |
title_sort | molecular genetics biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism with 41 tables |
topic | Enzymes deficiency Purine-Pyrimidine Metabolism, Inborn Errors genetics Purine-Pyrimidine Metabolism, Inborn Errors metabolism Purine-Pyrimidine Metabolism, Inborn Errors physiopathology Purines Metabolism Disorders Pyrimidines Metabolism Disorders Molekulargenetik (DE-588)4039987-4 gnd Stoffwechselkrankheit (DE-588)4057700-4 gnd Pyrimidinstoffwechselstörung (DE-588)4321807-6 gnd Purinstoffwechsel (DE-588)4176403-1 gnd Angeborene Krankheit (DE-588)4331107-6 gnd Erbkrankheit (DE-588)4015106-2 gnd Pyrimidinstoffwechsel (DE-588)4195173-6 gnd Purinstoffwechselstörung (DE-588)4205704-8 gnd Physiologische Chemie (DE-588)4076124-1 gnd |
topic_facet | Enzymes deficiency Purine-Pyrimidine Metabolism, Inborn Errors genetics Purine-Pyrimidine Metabolism, Inborn Errors metabolism Purine-Pyrimidine Metabolism, Inborn Errors physiopathology Purines Metabolism Disorders Pyrimidines Metabolism Disorders Molekulargenetik Stoffwechselkrankheit Pyrimidinstoffwechselstörung Purinstoffwechsel Angeborene Krankheit Erbkrankheit Pyrimidinstoffwechsel Purinstoffwechselstörung Physiologische Chemie Konferenzschrift 1991 München |
work_keys_str_mv | AT gresserursula moleculargeneticsbiochemistryandclinicalaspectsofinheriteddisordersofpurineandpyrimidinemetabolismwith41tables AT abreurade moleculargeneticsbiochemistryandclinicalaspectsofinheriteddisordersofpurineandpyrimidinemetabolismwith41tables |