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A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient.

International journal of dermatology - 1 Jun 2015

Ayoub Nedhal, Al-Khenaizan Sultan, Sonbol Haitham, Albreakan Rakan, AlSufyani Mohammed, AlBalwi Mohammed

Abstract excerpt

No abstract is available from the source.

Topics

Homozygote
Humans
Male
Mutation
Organic Anion Transporters
Osteoarthropathy, Primary Hypertrophic
Phenotype
Saudi Arabia
Severity of Illness Index
Young Adult

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25601417
DOI: 10.1111/ijd.12770

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient.PMID 25601417Read ↗

Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients.Semantic proximity Read ↗

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A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

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

Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

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