Identification of modifying pathways involved in the phenotypic variability of spinal muscular atrophy (SMA).

被引：0
|
作者：
Helmken, C
Hofmann, Y
Raschke, H
Rudnik-Schöneborn, S
Zerres, K
Wirth, B
机构：
[1] Inst Human Genet, Dept Mol Genet, Bonn, Germany
[2] Inst Human Genet, Aachen, Germany
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2002年 / 71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：
2133
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收藏
页码：534 / 534
页数：1
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