Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Abstract Background Asthenozoospermia is one of the most common causes of male infertility, and its genetic etiology is poorly understood. DNAH9 is a core component of outer dynein arms in cilia and flagellum. It was reported that variants of DNAH9 (OMIM: 603330) might cause primary ciliary dyskines...

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Bibliographic Details
Main Authors: Dongdong Tang, Yanwei Sha, Yang Gao, Jingjing Zhang, Huiru Cheng, Junqiang Zhang, Xiaoqing Ni, Chao Wang, Chuan Xu, Hao Geng, Xiaojin He, Yunxia Cao
Format: Article
Language:English
Published: BMC 2021-02-01
Series:Reproductive Biology and Endocrinology
Subjects:
Asthenozoospermia
Nonsyndromic
Flagellum
DNAH9
ICSI
Online Access:https://doi.org/10.1186/s12958-021-00709-0

Internet

https://doi.org/10.1186/s12958-021-00709-0

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