血红蛋白病
溶血
医学
DNA
分子生物学
BETA(编程语言)
遗传学
基因组DNA
基因组不稳定性
核苷酸
基因
免疫学
溶血性贫血
DNA损伤
生物
程序设计语言
计算机科学
作者
Scimè-Degani,G Ivaldi,Maria Baffico,Daniela Leone,Maria Isola Parodi,D Pascotto,Francesca Garofalo,Emma Rabino‐Massa
出处
期刊:PubMed
日期:2001-06-01
卷期号:43 (2): 135-8
摘要
A young woman aged 21 was found to be a new carrier of Hb-Belfast: beta 15 (A 12) Trp-->Arg, and the characteristics of her hemoglobinopathy were not different from those of the four cases so far described: mild hemolysis with molecular instability of the abnormal Hb, red cells inclusion bodies, and slight alterations of some functional parameters of whole blood. On this occasion, direct DNA analysis indicated the genomic nucleotide replacement of the disease: TGG-AGG. This was inherited by the mother, originating from Bari (Apulia).
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