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

Dongfeng GengHongguo ZhangXiangyin LiuJia FeiYuting JiangRuizhi Liu Ruixue WangGuirong Zhang

Published in: Journal of clinical laboratory analysis (2019)

Our study revealed three heterozygous missense variants in KISS1R which expanded the mutation spectrum of KISS1R in infertile men with NOA in the northeast of China.

Keyphrases

early onset
intellectual disability
single cell
gene expression
middle aged
skeletal muscle
dna methylation
autism spectrum disorder