Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human

Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human

Abstract Background 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. Methods Whole‐exome sequencing was perform...

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Bibliographic Details
Main Authors: Yuanyuan Ye, Xiaoli Wei, Yanwei Sha, Na Li, Xiaohong Yan, Ling Cheng, Duanrui Qiao, Weidong Zhou, Rongfeng Wu, Qiaobin Liu, Youzhu Li
Format: Article
Language:English
Published: Wiley 2020-07-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
acephalic spermatozoa
frameshift mutation
TSGA10
whole‐exome sequencing
Online Access:https://doi.org/10.1002/mgg3.1284

Internet

https://doi.org/10.1002/mgg3.1284

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