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

Ayoub, N., Al-Khenaizan, S., Sonbol, H., Albreakan, R., Alsufyani, M., & Albalwi, M. (2015, June 1). A novel homozygous mutation in the SLCO2A1 gene is associated with severe primary hypertrophic osteoarthropathy phenotype in a Saudi patient. International Journal of Dermatology. Blackwell Publishing Ltd. https://doi.org/10.1111/ijd.12770