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24. Exome sequencing identifies compound heterozygous PKHD1 mutations as a cause of autosomal recessive polycystic kidney disease. Zhang D; Lu L; Yang HB; Li M; Sun H; Zeng ZP; Li XP; Xia WB; Xing XP Chin Med J (Engl); 2012 Jul; 125(14):2482-6. PubMed ID: 22882926 [TBL] [Abstract][Full Text] [Related]
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