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Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction.

Ann Noninvasive Electrocardiol · 2022 · PMC8739608 · PMID 34755423

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a decreasing trendno p-value reported
Physical and chemical parameter prediction of protein Compared with the amino acids of wild‐type KCNH2 (Table 3 ), KCNH2 p.307_308del showed a decreasing trend in molecular weight and increasing instability.

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