无精子症
不育
男性不育
表型
基因
生物
遗传学
突变
支持细胞
梗阻性无精症
内分泌学
精子发生
怀孕
作者
Toshinobu Miyamoto,Eitetsu Koh,Akira Tsujimura,Yasushi Miyagawa,Gaku Minase,Yuki Ueda,Mikio Namiki,Kazuo Sengoku
出处
期刊:Andrologia
[Wiley]
日期:2014-11-13
卷期号:47 (9): 1083-1085
被引量:1
摘要
A loss of function of the murine Sin3A gene resulted in male infertility with Sertoli cell-only syndrome (SCOS) phenotype in mice. Here, we investigated the relevance of this gene to human male infertility with azoospermia caused by SCOS. Mutation analysis of SIN3A in the coding region was performed on 80 Japanese patients. However, no variants could be detected. This study suggests a lack of association of SIN3A gene sequence variants with azoospermia caused by SCOS in humans.
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