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Identification of KISS1R gene mutations in disorders of non‐obstructive azoospermia in the northeast population of China

BACKGROUND: Non‐obstructive azoospermia (NOA), a serious phenotype of male spermatogenesis failure, is a multifactorial disease which is regulated by genetic, epigenetic, and environmental factors. Some gene structural variants have been demonstrated to be related to NOA. Loss‐of‐function mutations...

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Detalles Bibliográficos
Autores principales:	Geng, Dongfeng, Zhang, Hongguo, Liu, Xiangyin, Fei, Jia, Jiang, Yuting, Liu, Ruizhi, Wang, Ruixue, Zhang, Guirong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2019
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171332/ https://www.ncbi.nlm.nih.gov/pubmed/31821609 http://dx.doi.org/10.1002/jcla.23139

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