Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease

Gao, Y; Wu, H; Xu, YP; Shen, QS; Xu, C; Geng, H; Lv, MR; Tan, Q; Li, KK; Tang, DD; Song, B; Zhou, P; Wei, ZL; He, XJ; Cao, YX

He, XJ; Cao, YX (通讯作者)，Anhui Med Univ, Reprod Med Ctr, Dept Obstet & Gynecol, Affiliated Hosp 1, Hefei 230022, Peoples R China.

HUMAN MUTATION, 2022; 43 (3): 434

Abstract

To investigate the genetic cause of male infertility characterized by severe asthenozoospermia, two unrelated infertile men with severe asthenozoosper......

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