Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Haplotype analysis of the CFTR gene on normal and mutant CFTR genes.

Mutation research - 1 Jan 2000

Karimi Nasibeh, Bidemeshki Pour Ali, Alibakhshi Reza, Almasi Shekoufeh

Abstract excerpt

BACKGROUND: Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are responsible for Cystic Fibrosis (CF) disease. Since the distribution of polymorphisms varies among populations, a comparison between the frequency of CFTR polymorphisms in patients and healthy population may further identify their role in CF disease. The results obtained from this research may facilitate the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

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

Share to Haplotypes

Share to Mutation

Share to Phenotype

Share to Prognosis

Source

Identifiers

PMID: 32563932
DOI: 10.1016/j.mrfmmm.2020.111708

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

Haplotype analysis of the CFTR gene on normal and mutant CFTR genes.PMID 32563932Read ↗

CFTR haplotypes in northern Iranian population.Semantic proximity Read ↗

A haplotype framework for cystic fibrosis mutations in Iran.Semantic proximity Read ↗

Contribution of common CFTR variants (M470V, T854, and Q1463) to cystic fibrosis in Tunisia: haplotype analysis.Semantic proximity Read ↗

Analysis of cystic fibrosis gene mutations and associated haplotypes in the Croatian population.Semantic proximity Read ↗

Mutation and new polymorphisms insight in introns 11 to 14a of CFTR gene of northern Iranian cystic fibrosis patients.Semantic proximity Read ↗

Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients.Semantic proximity Read ↗

Reporting Two Novel Mutations in Two Iranian Families with Cystic Fibrosis, Molecular and Bioinformatic AnalysisSemantic proximity Read ↗

Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis.Semantic proximity Read ↗

Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.Semantic proximity Read ↗

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.Semantic proximity Read ↗

Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers.Semantic proximity Read ↗

Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.