Human Genome Epidemiology Literature Finder
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Query Trace: Asthenozoospermia and SEPT4[original query] |
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Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. Human mutation 2021 12 43 (3): 434-443. Gao Yang, Wu Huan, Xu Yuping, Shen Qunshan, Xu Chuan, Geng Hao, Lv Mingrong, Tan Qing, Li Kuokuo, Tang Dongdong, Song Bing, Zhou Ping, Wei Zhaolian, He Xiaojin, Cao Yunx |
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- Page last updated:Apr 22, 2024
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