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Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing.

The Journal of investigative dermatology - 1 Oct 2012

Busch Jutta, Frank Valeska, Bachmann Nadine, Otsuka Atoshi, Oji Vinzenz, Metze Dieter, Shah Krati, Danda Sumita, Watzer Bernhard, Traupe Heiko, Bolz Hanno J, Kabashima Kenji, Bergmann Carsten

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PMID: 22696055
DOI: 10.1038/jid.2012.146

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Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing.PMID 22696055Read ↗

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study.Semantic proximity Read ↗

Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing.Semantic proximity Read ↗

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

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

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

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

Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

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

A novel homozygous mutation in the SLCO2A1 gene causing pachydermoperiostosis: Efficacy of hydroxychloroquine treatment.Semantic proximity Read ↗

Digital clubbing as the predominant manifestation of hypertrophic osteoarthropathy caused by pathogenic variants in HPGD in three Indian families.Semantic proximity Read ↗

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

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.Semantic proximity Read ↗

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