The "Reunion" mutation is a complex rearrangement of the CYP21 genes and associated with the 2/3 of classic forms of 21-Hydroxylase Deficiency in the Island

被引：0
|
作者：
Fourmaintraux, A
Alessandri, JL
Tardy, V
Cartault, F
Morel, Y
机构：
[1] ARDPMHE, Dept Pediat, St Pierre, Reunion, France
[2] ARDPMHE, Dept Pediat, St Denis Messageries, Reunion, France
[3] Hop Debrousse, INSERM U329, Lyon, France
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2002年 / 10卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
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页码：252 / 252
页数：1
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