Li, X. (2023). CRISPR/Cas9-mediated gene repair in autologous T cells to treat familial hemophagocytic lymphohistiocytosis (FHL).
Chicago Style (17th ed.) CitationLi, Xun. CRISPR/Cas9-mediated Gene Repair in Autologous T Cells to Treat Familial Hemophagocytic Lymphohistiocytosis (FHL). Berlin, 2023.
MLA (9th ed.) CitationLi, Xun. CRISPR/Cas9-mediated Gene Repair in Autologous T Cells to Treat Familial Hemophagocytic Lymphohistiocytosis (FHL). 2023.
Warning: These citations may not always be 100% accurate.