A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNASer(UCN) genes in a patient with hearing impairment, diabetes and congenital visual loss
Keywords: Mitochondrial mutation; m.7445G>A; m.6498C>A; tRNASer(UCN); MT-CO1; Hearing loss; Diabetes;