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Article

The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.

Journal of assisted reproduction and genetics - 1 Feb 2020

Pashaei Mahdieh, Rahimi Bidgoli Mohammad Masoud, Zare-Abdollahi Davood, Najmabadi Hossein, Haji-Seyed-Javadi Ramona, Fatehi Farzad, Alavi Afagh

Abstract excerpt

PURPOSE: It is estimated that 40-50% of infertility among human couples is due to male infertility. Azoospermia is estimated to occur in 1% of all men and to be the cause of 10-20% of male infertility. Genetic defects, including single gene effects, maybe cause of azoospermia in 20-30% of affected males. Here, we aim to identify the genetic cause of azoospermia in a man who is also affected by hereditary spastic...

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Identifiers

PMID: 31916078
DOI: 10.1007/s10815-019-01660-1
PMCID: PMC7056785

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.PMID 31916078Read ↗

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