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62. Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction. Yang Z; Ma Y; Huang J; Xian J; Huang Y; Wu L; Zhu W; Wang F; Chen L; Lin X; Lin Y Ann Noninvasive Electrocardiol; 2022 Jan; 27(1):e12889. PubMed ID: 34755423 [TBL] [Abstract][Full Text] [Related]
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