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Article

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

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PMID: 25601417
DOI: 10.1111/ijd.12770

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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 ↗

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

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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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