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Article

Analysis of 31 CFTR mutations in 55 families from the South of Spain.

Early human development - 1 Nov 2001

Gómez-Llorente M A, Suarez A, Gómez-Llorente C, Muñoz A, Arauzo M, Antunez A, Navarro M, Gil A, Gómez-Capilla J A

Abstract excerpt

We carried out a molecular analysis of 350 chromosomes from 55 families originating from the South of Spain (Andalucia) who were diagnosed with cystic fibrosis (CF). We used polymerase chain reaction, followed by an oligonucleotide ligation assay (OLA) and sequence-coded separation using capillary electrophoresis. A frequency of 43.5% for DeltaF508 was found, making it the most common CF mutation in our sample....

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Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Electrophoresis, Capillary

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Share to Oligonucleotides

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Source

Identifiers

PMID: 11755047
DOI: 10.1016/s0378-3782(01)00218-3

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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