Literature DB >> 20950711

Exercise extreme caution when calling rare genetic variants novel arrhythmia syndrome susceptibility mutations.

Arthur A M Wilde, Michael J Ackerman.   

Abstract

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Year:  2010        PMID： 20950711     DOI： 10.1016/j.hrthm.2010.10.008

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN： 1547-5271            Impact factor:   6.343


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  4 in total

1.  Functional characterization of CaVα2δ mutations associated with sudden cardiac death.

Authors:  Benoîte Bourdin; Behzad Shakeri; Marie-Philippe Tétreault; Rémy Sauvé; Sylvie Lesage; Lucie Parent
Journal:  J Biol Chem       Date:  2014-12-19       Impact factor: 5.157

Review 2.  Genetics of Brugada syndrome.

Authors:  Jyh-Ming Jimmy Juang; Minoru Horie
Journal:  J Arrhythm       Date:  2016-09-12

Review 3.  Ion Channel Disorders and Sudden Cardiac Death.

Authors:  Anna Garcia-Elias; Begoña Benito
Journal:  Int J Mol Sci       Date:  2018-02-28       Impact factor: 5.923

4.  Diagnostic accuracy of the response to the brief tachycardia provoked by standing in children suspected for long QT syndrome.

Authors:  Arja S Vink; Ben J M Hermans; Joana Pimenta; Puck J Peltenburg; Luc H P M Filippini; Nynke Hofman; Sally-Ann B Clur; Nico A Blom; Arthur A M Wilde; Tammo Delhaas; Pieter G Postema
Journal:  Heart Rhythm O2       Date:  2021-03-13
  4 in total

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