1995•Pediatric NeurologyRequires access

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome

Yolanda Campos, Teresa Garcı́a-Silva, Carlos R. Barrionuevo, Ana Cabello, Rafael Muley, Joaquı́n Arenas

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Key concepts: Heteroplasmy, MELAS syndrome, Mitochondrial encephalomyopathy, Lactic acidosis, Mitochondrial myopathy, Mitochondrial DNA, Kearns–Sayre syndrome, Muscle biopsy

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Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome — Research Paper | ScholarLens