在一个患有孤立非阻塞性亚精子症的男性中,复合异质合体KCTD19变体
Yuki Muranishi1,2, Yuko Katoh-Fukui1, Atsushi Hattori1
1Department of Molecular Endocrinology National Research Institute for Child Health and Development Tokyo Japan.
Reproductive medicine and biology
|September 25, 2024
概括
在KCTD19基因的罕见变异导致非阻塞性精症 (NOA),男性不育的一种形式. 这项研究在NOA.患者中确定了KCTD19中的复合异合体变体.
科学领域:
- 遗传学 遗传学 是一个
- 生殖生物学 生殖生物学
- 人类分子遗传学 人类分子遗传学
背景情况:
- 非阻塞性精子缺血症 (NOA) 是一种严重的男性不孕症,其遗传原因基本上尚不清楚.
- 基因查对于识别涉及精子生成失败的新基因至关重要.
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