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Article

Analysis of five CFTR mutations in Hungarian cystic fibrosis patients.

Journal of inherited metabolic disease - 1 Jan 1996

Németh K, Fekete G, Kiss E, Váradi A, Holics K, Ujhelyi R

Abstract excerpt

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Topics

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Share to Cystic Fibrosis

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

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Source

Identifiers

PMID: 8803789
DOI: 10.1007/BF01799276

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

Analysis of five CFTR mutations in Hungarian cystic fibrosis patients.PMID 8803789Read ↗

A comprehensive CFTR mutation analysis of German cystic fibrosis patients.Semantic proximity Read ↗

Multimutational analysis of eleven cystic fibrosis mutations common in the Mediterranean areas.Semantic proximity Read ↗

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.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 ↗

Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations.Semantic proximity Read ↗

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

Mutations of the CFTR gene and novel variants in Turkish patients with cystic fibrosis: 24-years experience.Semantic proximity Read ↗

The pathogenic consequences of a single mutated CFTR gene.Semantic proximity Read ↗

Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG).Semantic proximity Read ↗

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

Study of 12 mutations in Turkish cystic fibrosis patients.Semantic proximity Read ↗

Mutation analysis of the CFTR gene in Slovak cystic fibrosis patients by DHPLC and subsequent sequencing: identification of four novel mutations.Semantic proximity Read ↗

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