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The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men.

Genes & genomics - 1 Apr 2023

Jafari Leyla, Safinejad Kyumars, Nasiri Mahboobeh, Heidari Mansour, Houshmand Massoud

Abstract excerpt

BACKGROUND: Male infertility due to very severe oligozoospermia has been associated with some genetic risk factors. OBJECTIVE: To investigate the distribution of the mutations in the CFTR gene, the CAG-repeat expansion of the AR gene, also Y chromosome microdeletions and karyotyping abnormalities in very severe oligozoospermia patients. METHODS: In the present case-control study, 200 patients and 200 fertile...

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Share to Cystic Fibrosis Transmembrane Conductance Regulator
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Multiplex Polymerase Chain Reaction

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PMID: 35982373
DOI: 10.1007/s13258-022-01300-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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