法国的血红蛋白病。
Hémoglobinopathies in France.
作者信息
Labie D, Galacteros F, Girot R, Rosa J
出版信息
Nouv Rev Fr Hematol (1978). 1986;28(4):253-5.
PMID:3774536
Abstract
A first approximation of the incidences of abnormal hemoglobin traits in France is given. The data include all the large ethnic minorities living in France, and also take into account the second and third generations. We estimate 1.3 X 10(5) and 1.8 X 10(5) individuals with HbS trait and beta-thalassemia trait respectively.
摘要
给出了法国异常血红蛋白特征发生率的初步近似值。数据涵盖了生活在法国的所有大型少数族裔，并且考虑到了第二代和第三代。我们估计分别有1.3×10⁵ 和1.8×10⁵ 个体具有血红蛋白S特征和β地中海贫血特征。
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