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Article

Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.

Human reproduction (Oxford, England) - 1 May 2009

Sharma N, Acharya N, Singh S K, Singh M, Sharma U, Prasad R

Abstract excerpt

BACKGROUND: Mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene can cause congenital bilateral absence of vas deferens. Yet, the spectrum and frequency of CFTR mutations in Indian males with congenital absence of vas deferens (CAVD) is unknown. METHODS: We investigate...

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Source

Identifiers

PMID: 19181743
DOI: 10.1093/humrep/den500

Genes

CFTR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19181743-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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