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8. Whole-exome sequencing identifies rare compound heterozygous mutations in the MYBPC3 gene associated with severe familial hypertrophic cardiomyopathy. Zhou N; Qin S; Liu Y; Tang L; Zhao W; Pan C; Qiu Z; Wang X; Shu X Eur J Med Genet; 2018 Aug; 61(8):434-441. PubMed ID: 29524613 [TBL] [Abstract][Full Text] [Related]
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