{"title":"更正 \"短 QT 综合征:诊断和管理的现有证据\"","authors":"","doi":"10.1002/joa3.13043","DOIUrl":null,"url":null,"abstract":"<p>Dewi IP, Dharmadjati BB. Short QT syndrome: The current evidences of diagnosis and management. J Arrhythm. 2020;36(6):962–966.</p><p>In the third paragraph of the “Introduction” section, we add “Due to its rarity and potential lethality, understanding the pathogenesis and clinical implications of SQTS is crucial. This literature review aims to provide a comprehensive and detailed overview of SQTS. Additionally, this article updates prior review by Reviriego et al.,<sup>a</sup> to incorporate the latest advancements and insights of SQTS.”</p><p>In the last paragraph of the “Genetic Factors in SQTS” section, we cite reference b at the end of the following sentence, as in “Templin et al, described another mutation in the CACNA2D1 gene that causes a decrease in the flow of Ca-type L channels (SQTS 6).<sup>b</sup>”</p><p>We add two citations as follows.</p><p>a. Reviriego SM, Merino JL. Short QT Syndrome. ESC Council for Cardiology Practice. 2010; 9(2).</p><p>b. Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, et al. Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). Eur Heart J. 2011;32(9):1077–88. https://doi.org/10.1093/eurheartj/ehr076</p><p>We apologize for these errors.</p>","PeriodicalId":15174,"journal":{"name":"Journal of Arrhythmia","volume":"40 3","pages":"653"},"PeriodicalIF":2.2000,"publicationDate":"2024-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/joa3.13043","citationCount":"0","resultStr":"{\"title\":\"Correction to “Short QT Syndrome: The Current Evidences of Diagnosis and Management”\",\"authors\":\"\",\"doi\":\"10.1002/joa3.13043\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Dewi IP, Dharmadjati BB. Short QT syndrome: The current evidences of diagnosis and management. J Arrhythm. 2020;36(6):962–966.</p><p>In the third paragraph of the “Introduction” section, we add “Due to its rarity and potential lethality, understanding the pathogenesis and clinical implications of SQTS is crucial. This literature review aims to provide a comprehensive and detailed overview of SQTS. Additionally, this article updates prior review by Reviriego et al.,<sup>a</sup> to incorporate the latest advancements and insights of SQTS.”</p><p>In the last paragraph of the “Genetic Factors in SQTS” section, we cite reference b at the end of the following sentence, as in “Templin et al, described another mutation in the CACNA2D1 gene that causes a decrease in the flow of Ca-type L channels (SQTS 6).<sup>b</sup>”</p><p>We add two citations as follows.</p><p>a. Reviriego SM, Merino JL. Short QT Syndrome. ESC Council for Cardiology Practice. 2010; 9(2).</p><p>b. Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, et al. Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). Eur Heart J. 2011;32(9):1077–88. https://doi.org/10.1093/eurheartj/ehr076</p><p>We apologize for these errors.</p>\",\"PeriodicalId\":15174,\"journal\":{\"name\":\"Journal of Arrhythmia\",\"volume\":\"40 3\",\"pages\":\"653\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-05-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/joa3.13043\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Arrhythmia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/joa3.13043\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Arrhythmia","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/joa3.13043","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
Dewi IP, Dharmadjati BB.短 QT 综合征:当前诊断和管理的证据。J Arrhythm.2020;36(6):962-966.在 "引言 "部分的第三段,我们添加了 "由于其罕见性和潜在致死性,了解 SQTS 的发病机制和临床意义至关重要。本文献综述旨在提供有关 SQTS 的全面而详细的概述。此外,本文更新了 Reviriego 等人之前的综述,a 纳入了有关 SQTS 的最新进展和见解。"在 "SQTS 的遗传因素 "部分的最后一段,我们在以下句子的末尾引用了参考文献 b,如 "Templin 等人描述了 CACNA2D1 基因的另一种突变,这种突变会导致 Ca 型 L 通道流量减少(SQTS 6)。"我们添加了以下两个引文:a. Reviriego SM, Merino JL.短 QT 综合征。ESC心脏病学实践委员会。2010; 9(2).b. Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, et al. Identification of a new loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6).Eur Heart J. 2011; 32(9):1077-88. https://doi.org/10.1093/eurheartj/ehr076We 对这些错误深表歉意。
Correction to “Short QT Syndrome: The Current Evidences of Diagnosis and Management”
Dewi IP, Dharmadjati BB. Short QT syndrome: The current evidences of diagnosis and management. J Arrhythm. 2020;36(6):962–966.
In the third paragraph of the “Introduction” section, we add “Due to its rarity and potential lethality, understanding the pathogenesis and clinical implications of SQTS is crucial. This literature review aims to provide a comprehensive and detailed overview of SQTS. Additionally, this article updates prior review by Reviriego et al.,a to incorporate the latest advancements and insights of SQTS.”
In the last paragraph of the “Genetic Factors in SQTS” section, we cite reference b at the end of the following sentence, as in “Templin et al, described another mutation in the CACNA2D1 gene that causes a decrease in the flow of Ca-type L channels (SQTS 6).b”
We add two citations as follows.
a. Reviriego SM, Merino JL. Short QT Syndrome. ESC Council for Cardiology Practice. 2010; 9(2).
b. Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, et al. Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). Eur Heart J. 2011;32(9):1077–88. https://doi.org/10.1093/eurheartj/ehr076