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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Cardiac defects in RASopathies: a review of genotype- phenotype correlations
I Loddo1, M C Cutrupi2, D Concolino3
1Diagnostic and Therapeutic Services Department - Clinical Pathology, Microbiology and Virology Laboratory - Medical Genetics Unit. IRCCS - ISMETT (Mediterranean Institute for Transplantation and Advanced Specialized Therapies) Palermo, Italy.
Journal of Biological Regulators and Homeostatic Agents
|October 1, 2020
Abstract
No abstract available in PubMed .
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