Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family

Overview of attention for article published in Journal of Endocrinological Investigation, April 2019

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DHLangbecker #digitalhealth #update Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family. https://t.co/pSf1OlnLpS

21 Apr 2019

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