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  6. Role of risk stratification and genetics in sudden cardiac death
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  7. Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing
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  8. When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review
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  9. Pathogenicity of the Homoplasmic m.8701A>G Variant Requires Confirmation
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