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

Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.

Journal of Korean medical science - 1 Feb 2005

Ahn Kang Mo, Park Hwa Young, Lee Ji Hyun, Lee Min Goo, Kim Jeong Ho, Kang Im Ju, Lee Sang Il

Abstract excerpt

Cystic fibrosis (CF) is inherited as an autosomal recessive trait, and the mutations in cystic fibrosis transmembrane conductance regulator (CFTR) gene contributes to the CF syndrome. Although CF is common in Caucasians, it is known to be rare in Asians. Recently, we experienced two cases of CF i...

Read the complete abstract on PubMed

Topics

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

Share to Bronchiectasis
Share to Cough
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pancreas

Share to Sinusitis

Share to Tomography, X-Ray Computed

Source

Open in PubMed Open full text

Identifiers

PMID: 15716623
DOI: 10.3346/jkms.2005.20.1.153
PMCID: PMC2808565

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15716623-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.PMID 15716623Read ↗

The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis.Semantic proximity Read ↗

Four case reports of Chinese cystic fibrosis patients and literature review.Semantic proximity Read ↗

Clinical and genetic characteristics of diseases caused by CFTR gene mutations in 15 Chinese children: a retrospective analysis.Semantic proximity Read ↗

[Molecular diagnosis of two Chinese cystic fibrosis children and literature review].Semantic proximity Read ↗

Clinical characterization and diagnosis of cystic fibrosis through exome sequencing in Chinese infants with Bartter-syndrome-like hypokalemia alkalosis.Semantic proximity Read ↗

Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported casesSemantic proximity Read ↗

Clinical Phenotypes and Genotypic Spectrum of Cystic Fibrosis in Chinese Children.Semantic proximity Read ↗

Characterization of gene mutations and phenotypes of cystic fibrosis in Chinese patients.Semantic proximity Read ↗

Report of a Korean patient with cystic fibrosis, carrying Q98R and Q220X mutations in the CFTR gene.Semantic proximity Read ↗

Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis.Semantic proximity Read ↗

Molecular diagnosis of cystic fibrosis in Indian patients--a preliminary report.Semantic proximity Read ↗

Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosisSemantic proximity Read ↗

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