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

Can a place of origin of the main cystic fibrosis mutations be identified?

American journal of human genetics - 1 Jan 2002

Mateu Eva, Calafell Francesc, Ramos Maria Dolors, Casals Teresa, Bertranpetit Jaume

Abstract excerpt

The genetic background of the mutations that most often cause cystic fibrosis (CF) is different from that of non-CF chromosomes in populations of European origin. It is not known whether these haplotype backgrounds could be found at high frequencies in populations in which CF is, at present, not common; such populations would be candidates for the place of origin of CF mutations. An analysis of haplotypes of CF...

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Emigration and Immigration

Share to Europe

Share to Introns

Share to Likelihood Functions

Share to Microsatellite Repeats

Share to Sample Size

Source

Open in PubMed Open full text

Identifiers

PMID: 11713719
DOI: 10.1086/338243
PMCID: PMC384895

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Can a place of origin of the main cystic fibrosis mutations be identified?PMID 11713719Read ↗

The geographic distribution of cystic fibrosis mutations gives clues about population origins.Semantic proximity Read ↗

Geographic distribution and origin of CFTR mutations in Germany.Semantic proximity Read ↗

The origin of the major cystic fibrosis mutation (delta F508) in European populations.Semantic proximity Read ↗

G542X as a probable Phoenician cystic fibrosis mutation.Semantic proximity Read ↗

Worldwide genetic analysis of the CFTR region.Semantic proximity Read ↗

Genetic and geographical variability in cystic fibrosis: evolutionary considerations.Semantic proximity Read ↗

A more detailed map of the cystic fibrosis mutation DF508 frequencies in Europe.Semantic proximity Read ↗

Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution.Semantic proximity Read ↗

Characterization Of Ancestral Origin Of Cystic Fibrosis Of Patients With New Reported Mutations In CFTRSemantic proximity Read ↗

Sequence of deltaF508 CFTR allele identified at present is lacking in medieval specimens from Central Poland. Preliminary results.Semantic proximity Read ↗

Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosisSemantic proximity Read ↗

Characterization of Ancestral Origin of Cystic Fibrosis of Patients with New Reported Mutations in CFTR.Semantic proximity Read ↗

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