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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Personalized medicine: genetic diagnosis for inherited cardiomyopathies/channelopathies

Michael J Ackerman1, Cherisse A Marcou1, David J Tester1

  • 1Departments of Medicine (Division of Cardiovacular Diseases), Pediatrics (Division of Pediatric Cardiology), and Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, Minnesota, United States.

Revista Espanola De Cardiologia (English Ed.)
|April 30, 2014
PubMed

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