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A distinct molecular mechanism by which phenytoin rescues a novel long QT 3 variant

  • Published:2020-07 Issue: Volume:144 Page:1-11
  • ISSN:0022-2828
  • Container-title:Journal of Molecular and Cellular Cardiology
  • language:en
  • Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Gando Ivan,Campana Chiara,Tan Reina Bianca,Cecchin Frank,Sobie Eric A.,Coetzee William A.

Funder

NYU

Seventh Masonic District Association, Inc.

National Institutes of Health

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference38 articles.

1. Molecular pathophysiology of congenital long QT syndrome;Bohnen;Physiol. Rev.,2017

2. An international, multicentered, evidence-based reappraisal of genes reported to cause congenital long QT syndrome;Adler;Circulation,2020

3. Sodium channel mutations and arrhythmias;Ruan;Nat. Rev. Cardiol.,2009

4. Complexity of ranolazine and phenytoin use in an infant with long QT syndrome type 3;Tan;Heart Rhythm Case Rep.,2017

5. Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia;Wang;Hum. Mol. Genet.,1995

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