CCDC9 is identified as a novel candidate gene of severe asthenozoospermia-Reference-Cited by-同舟云学术

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia

Published:2019-09-10 Issue:6 Volume:65 Page:465-473
ISSN:1939-6368
Container-title:Systems Biology in Reproductive Medicine
language:en
Short-container-title:Systems Biology in Reproductive Medicine

Author:

Sha Yanwei¹,Xu Yankai²,Wei Xiaoli³,Liu Wensheng³^ORCID,Mei Libin¹,Lin Shaobin¹,Ji Zhiyong¹,Wang Xu¹,Su Zhiying¹,Qiu Pingping¹,Chen Jing¹^ORCID,Wang Xiong⁴

Affiliation:

1. Department of Andrology, United Diagnostic and Research Center for Clinical Genetics, School of Public Health & Women and Children’s Hospital, Xiamen University, Xiamen, Fujian, China

2. Department of Urology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, Shandong, China

3. School of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian, China

4. Reproductive Medicine Center, Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shandong, China

Publisher

Informa UK Limited

Subject

Urology,Reproductive Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/19396368.2019.1655812

Reference49 articles.

1. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice

2. Nonsense Mutation in Coiled-Coil Domain Containing 151 Gene (CCDC151) Causes Primary Ciliary Dyskinesia