
A novel m.3395AÂ >Â G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316AÂ >Â G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
Keywords: از دست دادن شنوایی; m.3395AÂ >Â G; m.4316AÂ >Â G; ND1 gene; tRNAIle gene; Cardiomyopathy; Hearing loss;