An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family-Reference-Cited by-同舟云学术

An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family

Published:2020-02-10 Issue:5 Volume:97 Page:741-746
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Tu Chaofeng¹²³,Wang Ying¹²,Nie Hongchuan¹²,Meng Lanlan²,Wang Weili¹,Li Yong¹,Li Dongyan¹,Zhang Huan²,Lu Guangxiu²,Lin Ge¹²,Tan Yue‐Qiu¹²^ORCID,Du Juan¹²

Affiliation:

1. Institute of Reproductive and Stem Cell EngineeringSchool of Basic Medical Science, Central South University Changsha China

2. Reproductive and Genetic Hospital of CITIC‐Xiangya Changsha China

3. Key Lab of MOE for Development Biology and Protein Chemistry, The Center for Heart Development, College of Life SciencesHunan Normal University Changsha China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13712

Reference18 articles.

1. Male infertility

2. A unique view on male infertility around the globe

3. World Health Organization reference values for human semen characteristics*‡

4. Review of Azoospermia

5. Control of mammalian germ cell entry into meiosis

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