Brain atrophy in a patient with mitochondrial DNA G8363A mutation
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DOI: 10.1097/cm9.0000000000000395
Abstract: The patient’s clinical symptoms improved after treatment To the Editor: Mitochondrial diseases are a common group of human genetic diseases that can occur at any with vitamins, lipoic acid, and coenzymes. However, he decade of… read more here.
Keywords: dna g8363a; dna; patient mitochondrial; brain atrophy ... See more keywords