Clinical and biochemical characteristics of 12 Chinese primary hypertrophic osteoarthropathy patients with HPGD mutations
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DOI: 10.7150/ijbs.71261
Abstract: Primary hypertrophic osteoarthropathy (PHO) is a rare genetic disease mainly affecting the skeletal and skin. Two genes involved in prostaglandin degradation are known to be responsible for PHO: HPGD and SLCO2A1. HPGD gene mutation can… read more here.
Keywords: hpgd mutations; clinical biochemical; primary hypertrophic; phoar1 patients ... See more keywords