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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Mol Genet Genomic Med
Main Authors: Li, Leilei, Wang, Ruixue, Yu, Yang, Zhang, Hongguo, Jiang, Yuting, Yang, Xiao, Liu, Ruizhi
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2020
Fag:
Original Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7503206/
https://ncbi.nlm.nih.gov/pubmed/32573075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1372
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker