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Article

Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population.

Human molecular genetics - 1 Jul 1992

Cuppens H, Loumi O, Marynen P, Cassiman J J

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Share to Algeria
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Frameshift Mutation

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

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Share to Multigene Family

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Source

Identifiers

PMID: 1284627
DOI: 10.1093/hmg/1.4.283

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population.PMID 1284627Read ↗

Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient.Semantic proximity Read ↗

CFTR mutations in the Algerian population.Semantic proximity Read ↗

Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->A.Semantic proximity Read ↗

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Analysis of five CFTR mutations in Hungarian cystic fibrosis patients.Semantic proximity Read ↗

A donor splice site mutation (1811 + 1G-->C) in intron 11 of the CFTR gene identified in a patient of Macedonian origin.Semantic proximity Read ↗

A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island.Semantic proximity Read ↗

Identification of three novel mutations in the CFTR gene, R117P, deltaD192, and 3121-1G-->A in four French patients.Semantic proximity Read ↗

G1244V: a novel missense mutation in exon 20 of the CFTR gene in a Bulgarian cystic fibrosis patient.Semantic proximity Read ↗

Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR geneSemantic proximity Read ↗

Identification of three novel mutations in the cystic fibrosis transmembrane conductance regulator gene in Argentinian CF patients.Semantic proximity Read ↗

Two novel frame shift mutations of CFTR causing null alleles in a patient with a severe course of CF.Semantic proximity Read ↗

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