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Article

Worldwide genetic analysis of the CFTR region.

American journal of human genetics - 1 Jan 2001

Mateu E, Calafell F, Lao O, Bonné-Tamir B, Kidd J R, Pakstis A, Kidd K K, Bertranpetit J

Abstract excerpt

Mutations at the cystic fibrosis transmembrane conductance regulator gene (CFTR) cause cystic fibrosis, the most prevalent severe genetic disorder in individuals of European descent. We have analyzed normal allele and haplotype variation at four short tandem repeat polymorphisms (STRPs) and two single-nucleotide polymorphisms (SNPs) in CFTR in 18 worldwide population samples, comprising a total of 1,944...

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Source

Open in PubMed Open full text

Identifiers

PMID: 11104661
DOI: 10.1086/316940
PMCID: PMC1234903

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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