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Article

Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia.

Journal of medical genetics - 1 Apr 2014

Ayhan Özgecan, Balkan Mahmut, Guven Ayse, Hazan Renin, Atar Murat, Tok Atalay, Tolun Aslıhan

Abstract excerpt

BACKGROUND: Azoospermia is the absence of a measurable level of spermatozoa in the semen. It affects approximately 1% of all men, and the genetic basis of the majority of idiopathic cases is unknown. We investigated two unrelated consanguineous families with idiopathic azoospermia. In family 1, there were three azoospermic brothers and one oligozoospermic brother; and in family 2, there were three azoospermic...

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Source

Identifiers

PMID: 24431330
DOI: 10.1136/jmedgenet-2013-102102

Genes

ZMYND15

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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