A rare mutation in MYH7 gene occurs with overlapping phenotype
Keywords: MYH7; Left ventricular non-compation; Cardiomyopathy; FTD; Laing Distal Myopathy; Overlapping syndrome; ACTA1; actin 1; CPK; creatine phosphokinase; CFTD; Congenital Fiber Type Disproportion; COX; cytochrome C oxidase; DES; desmin; EMG; electromyography;