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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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Subclinical cardiological involvement in Sicilian patients with pure congenital muscular dystrophy

R Falsaperla1, G Romeo, C Mattia

  • 1Department of Pediatrics, University of Catania, Catania, Italy. raffaelefalsaperla@hotmail.com

Minerva Pediatrica
|October 6, 2005
PubMed
Abstract

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