Ricardo Alves-Pinto, Tânia Proença, Miguel Martins-Carvalho, Paula Dias, Ana P Machado, Filipe Macedo
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引用次数: 0
Abstract
We present a case of a 34-year-old female with Hypertrophic Cardiomyopathy (HCM) without family history of HCM or sudden cardiac death, diagnosed 13 years earlier with a mutation in TNNC1 gene (ALA8VAL substitution, encoding troponin C protein).
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