溶血
突变
点突变
溶血性贫血
遗传学
编码区
DNA测序
血红蛋白
生物
DNA
基因
突变体
血红蛋白变体
分子生物学
化学
生物化学
免疫学
作者
Maya von Planta,James R. Humbert,Pierre Wacker,Peter C. Rimensberger,R Darbellay,Eddy Roosnek,Y Heller,P Beris
出处
期刊:PubMed
日期:2001-01-01
卷期号:2 (1): 61-6
被引量:4
标识
DOI:10.1038/sj/thj/6200085
摘要
So far, three different mutations at codon 42 of the beta-chain, and two at the corresponding position of the alpha-chain have been described, all leading to a hemolytic anemia. These mutations can either represent random phenomena occurring at an important location in the heme pocket, or may be secondary to the two highly homologous zones present in this region. These homologous zones may indicate a hot spot for point mutations created by abnormal crossing over or formation of loops, and an imperfect DNA repair process.
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