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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Pramod Kumar1, Ahmad Ghayas Ansari1, Deepa Sasikumar1
1Department of Cardiology, Sree Chitra Thirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.
Kelch-like family member 24 (KLHL24)-associated hypertrophic cardiomyopathy (HCM) presents unique risks. Early genetic testing guides timely interventions like implantable cardioverter-defibrillator (ICD) placement, even in low-risk patients.
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