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

[Identification of a HPGD mutation in three families affected with primary hypertrophic osteoarthropathy].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Apr 2018

Zhang Wanying, Wang Tao, Huang Shuaiwu, Zhao Xiuli

Abstract excerpt

OBJECTIVE: To detect mutation of HPGD gene among three pedigrees affected with primary hypertrophic osteoarthropathy (PHO) by DNA sequencing and high-resolution melting (HRM) analysis. METHODS: Genomic DNA was extracted from peripheral blood samples collected from the pedigrees. PCR and direct sequencing were carried out to identify potential mutations of the HPGD gene. Amplicons containing the mutation spot were...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Source

Identifiers

PMID: 29652982
DOI: 10.3760/cma.j.issn.1003-9406.2018.02.002

Genes

HPGD

Variants

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

[Identification of a HPGD mutation in three families affected with primary hypertrophic osteoarthropathy].PMID 29652982Read ↗

[Genetic analysis of a pedigree with primary hypertrophic osteoarthropathy].Semantic proximity Read ↗

[Genetic diagnosis for a Chinese Han family with primary hypertrophic osteoarthropathy].Semantic proximity Read ↗

[Genetic analysis of a child with Primary hypertrophic osteoarthropathy].Semantic proximity Read ↗

Clinical and biochemical characteristics of 12 Chinese primary hypertrophic osteoarthropathy patients with HPGD mutations.Semantic proximity Read ↗

A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy.Semantic proximity Read ↗

[Two cases of primary hypertrophic osteoarthropathy with SLCO2A1 gene mutations].Semantic proximity Read ↗

Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

[Mutation analysis for a pedigree affected with keratitis-ichthyosis-deafness syndrome].Semantic proximity Read ↗

Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up.Semantic proximity Read ↗

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