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Article

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

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PMID: 25810087
DOI: 10.1111/1346-8138.12856

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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 ↗

Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations.Semantic proximity Read ↗

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Pachydermoperiostosis in an African patient caused by a Chinese/Japanese SLCO2A1 mutation-case report and review of literature.Semantic proximity Read ↗

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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Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene.Semantic proximity Read ↗

[Progress in genetic research on pachydermoperiostosis].Semantic proximity Read ↗

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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