Various mechanisms cause RET-mediated signaling defects in Hirschsprung disease.

被引：0
|
作者：
Pelet, A
Geneste, O
Edery, P
Chappuis, S
Pasini, A
Attié, T
Munnich, A
Lenoir, G
Lyonnet, S
Billaud, M
机构：
[1] CNRS, UMR 5641, Genet Unit, F-69373 Lyon, France
[2] INSERM U393, Dept Genet, F-75743 Paris, France
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61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：
2006
引用
收藏
页码：A342 / A342
页数：1
相关论文
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    Pasini, A
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    Lenoir, G
    Lyonnet, S
    Billaud, M
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  • [10] Structural heart defects associated with ETB mutation, a cause of Hirschsprung disease
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    Croaker, Geoffrey D.
    [J]. BMC CARDIOVASCULAR DISORDERS, 2021, 21 (01)
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