Mutation analysis in families with X-linked metabolic disorders: adrenoleukodystrophy (X-ALD), ornithine carbamoyltransferase (OTC) deficiency and hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.

被引：0
|
作者：
Dvorakova, L [1 ]
Tietzeova, E [1 ]
Storkanova, G [1 ]
Zeman, J [1 ]
Hruba, E [1 ]
Kostalova, E [1 ]
Sebesta, I [1 ]
Kmoch, S [1 ]
Hrebicek, M [1 ]
机构：
[1] Inst Inherit Metab Disorders, Prague 2, Czech Republic
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
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暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
1705
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页码：473 / 473
页数：1
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