Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups:
Gespeichert in:
| Hauptverfasser: | , , , , , , , , |
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| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Erlangen ; Nürnberg
Friedrich-Alexander-Universität Erlangen-Nürnberg
2020
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| Schlagworte: | |
| Online-Zugang: | Volltext Volltext Volltext |
| Beschreibung: | 1 Online-Ressource |
| DOI: | 10.1186/s12881-020-01037-7 |
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| spelling | Assmann, Gunter Verfasser aut Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier Erlangen ; Nürnberg Friedrich-Alexander-Universität Erlangen-Nürnberg 2020 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Human genetics. Medical genetics. Cytogenetics. Human Genetics. Gene Function. Köhm, Michaela Verfasser aut Schuster, Volker Verfasser aut Behrens, Frank Verfasser aut Mössner, Rotraut Verfasser aut Magnolo, Nina Verfasser aut Oji, Vinzenz Verfasser aut Burkhardt, Harald Verfasser aut Hüffmeier, Ulrike Verfasser aut Sonderdruck aus BMC Medical Genetics Vol. 21 (2020) 10.1186/s12881-020-01037-7 https://doi.org/10.1186/s12881-020-01037-7 Resolving-System kostenfrei Volltext https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 Resolving-System kostenfrei Volltext https://open.fau.de/handle/openfau/14364 Verlag kostenfrei Volltext |
| spellingShingle | Assmann, Gunter Köhm, Michaela Schuster, Volker Behrens, Frank Mössner, Rotraut Magnolo, Nina Oji, Vinzenz Burkhardt, Harald Hüffmeier, Ulrike Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Human genetics. Medical genetics. Cytogenetics. |
| title | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_auth | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_exact_search | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_exact_search_txtP | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_full | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_fullStr | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_full_unstemmed | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_short | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_sort | genetic variants in fblim1 gene do not contribute to sapho syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| topic | Human genetics. Medical genetics. Cytogenetics. |
| topic_facet | Human genetics. Medical genetics. Cytogenetics. |
| url | https://doi.org/10.1186/s12881-020-01037-7 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 https://open.fau.de/handle/openfau/14364 |
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