[突尼斯的α地中海贫血：血红蛋白H病的分子基础]
[Alpha-thalassemia in Tunisia: molecular bases of hemoglobinosis H].
作者信息
Abbes S, Vidaud M, Fattoum S, Goossens M
出版信息
Nouv Rev Fr Hematol (1978). 1986;28(4):243-4.
PMID:3774533
Abstract
We report the study by restriction mapping of alpha genes in a case of Hb H disease in Tunisia. The genotype is: -alpha/-alpha which by itself is not usually responsible for the HbH phenotype. We postulate that the two remaining alpha genes are dysfunctional, this is under study.
摘要
我们报道了在突尼斯的一例血红蛋白H病（Hb H病）中通过α基因限制性图谱分析进行的研究。基因型为：-α/-α，其本身通常不会导致HbH表型。我们推测剩余的两个α基因功能异常，这一点正在研究中。
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