CHD7 missense variants and clinical characteristics of Chinese males with infertility

BACKGROUND: Isolated hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS) are rare genetic diseases that cause male infertility. The chromodomain helicase DNA‐binding protein 7 (CHD7) gene is commonly associated with KS and IHH. We speculated that CHD7 variants may be associated with male...

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Detalles Bibliográficos
Autores principales: Li, Leilei, Wang, Ruixue, Yu, Yang, Zhang, Hongguo, Jiang, Yuting, Yang, Xiao, Liu, Ruizhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503206/
https://www.ncbi.nlm.nih.gov/pubmed/32573075
http://dx.doi.org/10.1002/mgg3.1372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503206/
https://www.ncbi.nlm.nih.gov/pubmed/32573075
http://dx.doi.org/10.1002/mgg3.1372

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