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Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2020-05-15 , DOI: 10.1002/mgg3.1284 Yuanyuan Ye 1 , Xiaoli Wei 2 , Yanwei Sha 3 , Na Li 4 , Xiaohong Yan 1 , Ling Cheng 1 , Duanrui Qiao 5 , Weidong Zhou 1 , Rongfeng Wu 1 , Qiaobin Liu 6 , Youzhu Li 1
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2020-05-15 , DOI: 10.1002/mgg3.1284 Yuanyuan Ye 1 , Xiaoli Wei 2 , Yanwei Sha 3 , Na Li 4 , Xiaohong Yan 1 , Ling Cheng 1 , Duanrui Qiao 5 , Weidong Zhou 1 , Rongfeng Wu 1 , Qiaobin Liu 6 , Youzhu Li 1
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Acephalic spermatozoa is an extremely rare type of teratozoospermia that is associated with male infertility. Several genes have been reported to be relevant to acephalic spermatozoa. Thus, more genetic pathogenesis needs to be explored.
中文翻译：
TSGA10中的功能丧失突变会导致人类头型精子表型。
脑性精子症是一种罕见的畸形精子症，与男性不育有关。据报道，有几种基因与脑性精子有关。因此，需要探索更多的遗传发病机理。
更新日期：2020-07-06
中文翻译：
TSGA10中的功能丧失突变会导致人类头型精子表型。
脑性精子症是一种罕见的畸形精子症，与男性不育有关。据报道，有几种基因与脑性精子有关。因此，需要探索更多的遗传发病机理。
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