CHD7 missense variants and clinical characteristics of Chinese males with infertility

CHD7 missense variants and clinical characteristics of Chinese males with infertility

Abstract 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 wi...

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Bibliographic Details
Main Authors:	Leilei Li, Ruixue Wang, Yang Yu, Hongguo Zhang, Yuting Jiang, Xiao Yang, Ruizhi Liu
Format:	Article
Language:	English
Published:	Wiley 2020-09-01
Series:	Molecular Genetics & Genomic Medicine
Subjects:	chromodomain helicase DNA‐binding protein 7 male infertility missense variants targeted‐gene exome sequencing
Online Access:	https://doi.org/10.1002/mgg3.1372

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