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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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Genetic alterations of Carney complex are not present in sporadic cardiac myxomas

Franz Fogt1, Robert L Zimmerman, Christopher J Hartmann

  • 1Presbyterian Medical Center, University of Pennsylvania, Philadelphia, PA 19104, USA. fogt@mail.med.upenn.edu

International Journal of Molecular Medicine
|December 18, 2001
PubMed

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