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Article

Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family

14 Feb 2022

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Identifiers

PMID: 35176428
DOI: 10.1016/j.gene.2022.146281

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous familyPMID 35176428Read ↗

Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiencySemantic proximity Read ↗

Novel STAG3 variant causes oligoasthenoteratozoospermia with high sperm aneuploidy rateSemantic proximity Read ↗

Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency.Semantic proximity Read ↗

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A Long Contiguous Stretch of Homozygosity Disclosed a Novel STAG3 Biallelic Pathogenic Variant Causing Primary Ovarian Insufficiency: A Case Report and Review of the Literature.Semantic proximity Read ↗

A Long contiguous stretches of homozygosity disclosed a novel biallelic pathogenic variant in STAG3 causing Primary Ovarian InsufficiencySemantic proximity Read ↗

Analysis of STAG3 Mutations in Chinese Non-Obstructive Azoospermia Patients with Germ Cell Maturation ArrestSemantic proximity Read ↗

Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest.Semantic proximity Read ↗

Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencingSemantic proximity Read ↗

A novel ADGRG2 truncating variant associated with X-linked obstructive azoospermia in a large Chinese pedigree.Semantic proximity Read ↗

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