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Expression defect of the rare variant/Brugada mutation R1512W depends upon the SCN5A splice variant background and can be rescued by mexiletine and the common polymorphism H558R.
Hu, Rou-Mu; Song, Evelyn J; Tester, David J; Deschenes, Isabelle; Ackerman, Michael J; Makielski, Jonathan C; Tan, Bi-Hua.
Afiliación
  • Hu RM; Department of Cardiology, Heart Center & Beijing Key Laboratory of Hypertension, Beijing Chaoyang Hospital, Capital Medical University , Beijing, China.
  • Song EJ; Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin , Madison, WI, USA.
  • Tester DJ; Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, MD, USA.
  • Deschenes I; Departments of Medicine, Pediatrics, and Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester , MN, USA.
  • Ackerman MJ; Department of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, the Ohio State University , Columbus, OH, USA.
  • Makielski JC; Departments of Medicine, Pediatrics, and Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester , MN, USA.
  • Tan BH; Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin , Madison, WI, USA.
Channels (Austin) ; 15(1): 253-261, 2021 12.
Article en En | MEDLINE | ID: mdl-33535892

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mexiletine Límite: Humans Idioma: En Revista: Channels (Austin) Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mexiletine Límite: Humans Idioma: En Revista: Channels (Austin) Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos