Pathogenesis of Lethal Cardiac Arrhythmias in Mecp2 Mutant Mice: Implication for Therapy in Rett Syndrome

Author:

McCauley Mark D.12,Wang Tiannan1,Mike Elise1,Herrera Jose3,Beavers David L.12,Huang Teng-Wei4,Ward Christopher S.5,Skinner Steven6,Percy Alan K.7,Glaze Daniel G.8,Wehrens Xander H. T.123,Neul Jeffrey L.13459

Affiliation:

1. Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.

2. Department of Medicine (Cardiology), Baylor College of Medicine, Houston, TX 77030, USA.

3. Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX 77030, USA.

4. Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.

5. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

6. Greenwood Genetic Center, Greenwood, SC 29646, USA.

7. Department of Pediatrics (Neurology) and the Civitan International Research Center, University of Alabama, Birmingham, AL 35233, USA.

8. Department of Pediatrics (Neurology), Baylor College of Medicine, Houston, TX 77030, USA.

9. Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.

Abstract

Lethal ventricular arrhythmias in a mouse model of Rett syndrome can be prevented by phenytoin, which blocks a persistent sodium current.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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