Novel MEI1 compound heterozygous mutation in a sporadic family associated with spermatogenetic failure

Author:

Cui Yuan-Qing,Wang Xiong,Chen Jie,Li Feng-Hua,Xing Jin-Hao,Zhang Xue-Bao,Du Zhao-Li,Jin Yin-Shan

Publisher

Medknow

Subject

Urology,General Medicine

Reference13 articles.

1. Genetics of male infertility;Krausz;Nat Rev Urol,2018

2. Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure;Cannarella;Asian J Androl,2021

3. World Health Organization. WHO Laboratory Manual for the Examination and Processing of Human Semen. 5th ed. Geneva: WHO Press; 2010.

4. McGowan-Jordan J, Hastings RJ, Moore S, editors. ISCN 2020: An International System for Human Cytogenomic Nomenclature. Basel: Karger; 2020. p341–503.

5. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013;Krausz;Andrology,2014

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