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Article

CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France.

Human genetics - 1 Sept 1996

Claustres M, Desgeorges M, Moine P, Morral N, Estivill X

Abstract excerpt

In order to contribute to a better understanding of the dispersion of cystic fibrosis (CF) mutations in the South of France, seven diallelic and three multiallelic markers [three upstream of the cystic fibrosis transmembrane conductance regulator (CFTR) gene (XV-2c, KM 19 and J44) and seven intragenic polymorphism (IVS6A, IVS8CA, M470V, T854T, IVS17BTA, IVS17BCA and TUB18)] were analyzed for 143 delta F508...

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Source

Identifiers

PMID: 8707306
DOI: 10.1007/s004390050219

Genes

CFTR

Variants

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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