Mutations in a novel primate-specific cryptic exon of the LHCGR gene cause Leydig cell hypoplasia

被引：0
|
作者：
Kossack, N.
Simoni, M.
Richter-Unruh, A.
机构：
[1] Inst Reprod Med, Munster, Germany
[2] Endokrinol Ruhr, Bochum, Germany
来源：
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES | 2007年 / 115卷
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：S12 / S12
页数：1
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