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A novel homozygous mutation in the SLCO(2)A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient
Journal article   Peer reviewed

A novel homozygous mutation in the SLCO(2)A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient

Nedhal Ayoub, Sultan Al-Khenaizan, Haitham Sonbol, Rakan Albreakan, Mohammed AlSufyani and Mohammed AlBalwi
International journal of dermatology, Vol.54(6), pp.E233-E235
01/06/2015
PMID: 25601417

Abstract

Dermatology Life Sciences & Biomedicine Science & Technology

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