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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Evolving anatomic, functional, and molecular imaging in the early detection and prognosis of hypertrophic

Valentin Fuster1, Sarina van der Zee, Marc A Miller

  • 1Zena and Michael A. Wiener Cardiovascular Institute, and the Marie-Josee and Henry R. Kravis Cardiovascular Health Center, Mount Sinai Medical Center, The Mount Sinai School of Medicine, New York, NY, 10029, USA. valentin.fuster@mssm.edu

Journal of Cardiovascular Translational Research
|June 19, 2010
PubMed

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