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Article

CFTR mutation analysis of a Caucasian father with congenital bilateral absence of vas deferens, a Taiwanese mother, and twins resulting from ICSI procedure.

Journal of the Formosan Medical Association = Taiwan yi zhi - 1 Sept 2008

Chiang Han-Sun, Wu Chien-Chih, Wu Yi-No, Lu Jyh-Feng, Lin Gin-Hong, Hwang Jiann-Loung

Abstract excerpt

Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is one of the most common autosomal recessive diseases in Caucasians. We screened for the CFTR gene mutation in a Caucasian father with congenital bilateral absence of the vas deferen...

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Source

Identifiers

PMID: 18796364
DOI: 10.1016/S0929-6646(08)60119-9

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18796364-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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