Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleNovel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.AuthorsGao, 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, YunxiaPublicationHuman Mutation, 2022, Vol 43, Issue 3, p434ISSN1059-7794Publication typeArticleDOI10.1002/humu.24322