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Article

Gender-sensitive association of CFTR gene mutations and 5T allele emerging from a large survey on infertility.

Molecular human reproduction - 1 Aug 2005

Morea Antonella, Cameran Marilena, Rebuffi Anna Grazia, Marzenta Diana, Marangon Oriana, Picci Luigi, Zacchello Franco, Scarpa Maurizio

Abstract excerpt

Human infertility in relation to mutations affecting the cystic fibrosis transmembrane regulator (CFTR) gene has been investigated by different authors. The role of additional variants, such as the possible forms of the thymidine allele (5T, 7T and 9T) of the acceptor splice site of intron 8, has in some instances been considered. However, a large-scale analysis of the CFTR gene and number of thymidine residues,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16126774
DOI: 10.1093/molehr/gah214

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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