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Article

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

Journal of clinical laboratory analysis - 1 Apr 2020

Geng Dongfeng, Zhang Hongguo, Liu Xiangyin, Fei Jia, Jiang Yuting, Liu Ruizhi, Wang Ruixue, Zhang Guirong

Abstract excerpt

BACKGROUND: Non-obstructive azoospermia (NOA), a serious phenotype of male spermatogenesis failure, is a multifactorial disease which is regulated by genetic, epigenetic, and environmental factors. Some gene structural variants have been demonstrated to be related to NOA. Loss-of-function mutations of KISS1R cause normosmic idiopathic hypogonadotropic hypogonadism (IHH) which result in azoospermia at the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31821609
DOI: 10.1002/jcla.23139
PMCID: PMC7171332

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of KISS1R gene mutations in disorders of non-obstructive azoospermia in the northeast population of China.PMID 31821609Read ↗

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