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SEVERE LOSS-OF-FUNCTION SCN5A MUTATIONS ASSOCIATED WITH SINUS NODE DYSFUNCTION, ATRIAL ARRHYTHMIAS, AND POOR PACEMAKER CAPTURE

机译：与窦房结功能不全，房性心律失常和起搏器不良相关的严重功能丧失SCN5A突变

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Chiang David; Kim Jeffrey; Valdes Santiago; De La Uz Caridad; Fan Yuxin; Miyake Christina;
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1. Loss-of-Function SCN5A Mutations Associated With Sinus Node Dysfunction, Atrial Arrhythmias, and Poor Pacemaker Capture [J] . Chiang David Y., Kim Jeffrey J., Valdes Santiago O., Circulation. Arrhythmia and electrophysiology . 2015,第5期

机译：与窦房结功能障碍，房性心律不齐和起搏器捕获不良有关的功能丧失SCN5A突变
2. Cavotricuspid Isthmus Ablation and Subcutaneous Monitoring Device Implantation in a 2-Year-Old Baby with 2 SCN5A Mutations, Sinus Node Dysfunction, Atrial Flutter Recurrences, and Drug Induced Long-QT Syndrome: A Tricky Case of Pediatric Overlap Syndrome? [J] . De Filippo Paolo, Ferrari Paola, Iascone Maria, Journal of cardiovascular electrophysiology . 2015,第3期

机译：2岁婴儿的2个SCN5A突变，窦房结功能不全，房扑复发和药物诱发的长QT综合征的2岁婴儿中的针尖窦峡部消融和皮下监测设备植入：小儿重叠综合征的棘手案例？
3. Homozygous mutation in SCN5A associated with atrial quiescence, recalcitrant arrhythmias, and poor capture thresholds. [J] . Lopez KN, Decker JA, Friedman RA, Heart rhythm: the official journal of the Heart Rhythm Society . 2011,第3期

机译：SCN5A的纯合突变与心房静止，顽固性心律不齐和捕获阈值差有关。
4. Mechanism of Sinus Node Dysfunction in Carriers of the E161K Mutation in the SCN5A Gene [C] . Ronald Wilders Computing in Cardiology Conference . 2018

机译：SCN5A基因E161K突变携带者中窦房结功能障碍的机制
5. DNA mutation analysis of voltage-gated ion channel genes in two families with sick sinus syndrome and atrial fibrillation/AV nodal reentry tachycardia. [D] . Oh, Frances. 2010

机译：两个病态窦房结综合征和房颤/房室结折返性心动过速患者的电压门控离子通道基因的DNA突变分析。
6. Loss-of-Function SCN5A Mutations Associated With Sinus Node Dysfunction Atrial Arrhythmias and Poor Pacemaker Capture [O] . David Y. Chiang, Jeffrey J. Kim, Santiago O. Valdes, -1

机译：与窦房结功能障碍房性心律不齐和起搏器捕获不良有关的功能丧失SCN5A突变
7. CHARACTERIZATION OF COMPOUND HETEROZYGOSITY FOR MUTATIONS R269W IN KCNH2 AND P1824A IN SCN5A ASSOCIATED WITH LONG QT SYNDROME AND SINUS NODE DYSFUNCTION [O] . Hayashi Kenshi, Fujino Noboru, Uchiyama Katsuharu, 2011

机译：长QT综合征和窦房结功能障碍的SCN5A中KCNH2和P1824A突变R269W的复合杂化特征。

SEVERE LOSS-OF-FUNCTION SCN5A MUTATIONS ASSOCIATED WITH SINUS NODE DYSFUNCTION, ATRIAL ARRHYTHMIAS, AND POOR PACEMAKER CAPTURE

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