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Article

Detection of F508del mutation in cystic fibrosis transmembrane conductance regulator gene mutation among Malays.

Singapore medical journal - 1 Feb 2006

Zilfalil B A, Sarina S, Liza-Sharmini A T, Oldfield N J, Stenhouse S A

Abstract excerpt

INTRODUCTION: Cystic fibrosis (CF) is one of the common genetic disorders in the western world. It has been reported to be very rare in Asian populations. According to the Cystic Fibrosis Genetic Analysis Consortium, more than 1,000 mutations of the CF gene have been identified. The CF gene, named the cystic fibrosis transmembrane conductance regulator (CFTR), is located on chromosome 7 and composed of 27 exons....

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Identifiers

PMID: 16435054

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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