A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient

Publisher： John Wiley & Sons Inc

E-ISSN： 1365-4632|54|6|e233-e235

ISSN： 0011-9059

Source： INTERNATIONAL JOURNAL OF DERMATOLOGY, Vol.54, Iss.6, 2015-06, pp. : e233-e235

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