Related Experiment Video

Updated: Jun 12, 2025

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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Infantile Hypertrophic cardiomyopathy: steps towards an evidence-based approach to genetic testing

Gabrielle Norrish1,2, Juan Pablo Kaski3,4

  • 1Centre for Paediatric Inherited & Rare Cardiovascular Disease, Institute of Cardiovascular Science, London, UK.

Pediatric Research
|June 10, 2025
PubMed
Abstract

No abstract available in PubMed .

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