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Article

A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest.

Asian journal of andrology - 1 Sept 2009

Miyamoto Toshinobu, Tsujimura Akira, Miyagawa Yasushi, Koh Eitetsu, Sakugawa Naoko, Miyakawa Hiroe, Sato Hisashi, Namiki Mikio, Okuyama Akihiko, Sengoku Kazuo

Abstract excerpt

Genetic mechanisms have been implicated as a cause of some cases of male infertility. Recently, 10 novel genes involved in human spermatogenesis were identified by microarray analysis of human testicular tissue. One of these is spermatogenesis-associated 17 (SPATA17). To investigate whether defects in the SPATA17 gene are associated with azoospermia due to meiotic arrest, a mutational analysis was conducted, in...

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Source

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Identifiers

PMID: 19483714
DOI: 10.1038/aja.2009.30
PMCID: PMC3735008

Genes

SPATA17

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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