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4. Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family. Jiang Y; Du J; Song YW; Wang WB; Pang QQ; Li M; Wang O; Lian XL; Xing XP; Xia WB J Endocrinol Invest; 2019 Oct; 42(10):1245-1252. PubMed ID: 31004291 [TBL] [Abstract][Full Text] [Related]
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