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簡(jiǎn)要描述:Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular fu
產(chǎn)品型號(hào):bsm-62101R
廠商性質(zhì):生產(chǎn)廠家
更新時(shí)間:2025-03-03
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