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Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.

The Journal of dermatology - 1 Jun 2015

Kim Hee Joo, Koo Kyo Yeon, Shin Dong Youn, Kim Do Young, Lee Jin-Sung, Lee Min Geol

Abstract excerpt

No abstract is available from the source.

Topics

Humans
Male
Mutation
Organic Anion Transporters
Osteoarthropathy, Primary Hypertrophic
Republic of Korea
Siblings
Young Adult

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25810087
DOI: 10.1111/1346-8138.12856

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

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Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.PMID 25810087Read ↗

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Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene.Semantic proximity Read ↗

The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.Semantic proximity Read ↗

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Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.Semantic proximity Read ↗

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Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.Semantic proximity Read ↗

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