Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Yunhao LiYong LiYing WangLanlan MengChen TanJuan DuYue-Qiu TanHongchuan NieQianjun ZhangGuangxiu LuGe LinHuanzhu LiHuan ZhangChaofeng Tu

Published in: Journal of assisted reproduction and genetics (2022)

Our results extend the LRRC6 variant spectrum and provide reproductive guidance to families suffering from PCD-linked infertility caused by LRRC6 variants.

Keyphrases

copy number
polycystic ovary syndrome
intellectual disability
gene expression
dna methylation
genome wide
autism spectrum disorder
skeletal muscle
insulin resistance