Molecular prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency.

被引：0
|
作者：
Thuillier, L
Belbachir, H
Royer-Legrain, G
Attie-Bitach, T
Driben, A
Abadi, N
Kamoun, P
Saudubray, JM
Munnich, A
Bonnefont, JP
机构：
[1] Hop Necker Enfants Malad, Genet Biochem Unit, Paris, France
[2] Hop Necker Enfants Malad, Dept Genet, Paris, France
[3] Hop Necker Enfants Malad, Dept Pediat, Paris, France
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 65卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2442
引用
收藏
页码：A431 / A431
页数：1
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