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Article

Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.

Gynecologic and obstetric investigation - 1 Jan 2017

Colombo Roberto, Pontoglio Alessandro, Bini Maurizio

Abstract excerpt

AIM: Genetic investigations explain only a small percentage of cases of nonobstructive azoospermia (NOA), a condition that affects up to 2% of infertile couples. This study aimed to identify further genomic variants that are associated with primary spermatogenic failure within the testis. METHODS: One family with 2 infertile siblings affected by NOA was genotyped by whole-exome sequencing. DNA variants were...

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Source

Identifiers

PMID: 28355598
DOI: 10.1159/000468934

Genes

TEX15

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.PMID 28355598Read ↗

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Genetic variants in TEX15 gene conferred susceptibility to spermatogenic failure in the Chinese Han population.Semantic proximity Read ↗

Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han PopulationSemantic proximity Read ↗

A new TEX11 mutation causes azoospermia and testicular meiotic arrest.Semantic proximity Read ↗

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Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermiaSemantic proximity Read ↗

Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.Semantic proximity Read ↗

Genetic and functional analysis reveals novel mutations in meiotic genes underlying non-obstructive azoospermia.Semantic proximity Read ↗

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