Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance

DOI: 10.14744/AnatolJCardiol.2018.53258

Keywords: MT-ND5, whole-exome sequencing, cardiomyopathy, pulmonary hypertension

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Abstract:

The aim of the present study was to determine whether pathogenic mutations were present in families with mitochondrial cardiomyopathy that presented during adolescence

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