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- W4225258884 abstract "范科尼贫血（FA）是一种常染色体隐性、X连锁（FANCB基因突变）和常染色体显性（RAD51基因突变）遗传病，其发病机制是FA相关基因缺陷导致DNA损伤修复功能障碍，造成染色体自发断裂、错排、畸变等，从而出现骨髓衰竭、先天性畸形及肿瘤倾向等临床表现。本文主要针对其骨髓衰竭的发病机制进行综述。." @default.
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- W4225258884 date "2022-05-02" @default.
- W4225258884 modified "2023-09-23" @default.
- W4225258884 title "[Progress in pathogenesis of bone marrow failure in Fanconi anemia]." @default.
- W4225258884 doi "https://doi.org/10.3760/cma.j.cn112140-20211101-00917" @default.
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