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Updated: Apr 20, 2026

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Congenital myopathies: Rebuilding the natural history, one gene at a time
Enrico Bertini1, Basil T Darras2
1From the Unit of Neuromuscular and Neurodegenerative Disorders (E.B.), Laboratory of Molecular Medicine, Bambino Gesù Children's Research Hospital, Rome, Italy; and Department of Neurology (B.T.D.), Boston Children's Hospital and Harvard Medical School, Boston, MA. ebertini@gmail.com.
Neurology
|November 28, 2014
Abstract
No abstract available in PubMed .
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