- Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis
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Lee S, Park SY, Kwon HJ, Lee CH, Kim OH, Rhee Y
- KMID: 2373671
- J Korean Med Sci.
- 2016 May;31(5):735-742.
- doi: 10.3346/jkms.2016.31.5.735
Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare genetic disease affecting both skin and bones. Both autosomal dominant with incomplete penetrance and recessive inheritance of PDP have been previously... -
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