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2000•Neuromuscular DisordersRequires access

A mitochondrial tRNALys gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

Yolanda Campos, Gustavo Lorenzo, Miguel Á. Martín, Alicia Torregrosa, Pilar del Hoyo, Carlos Rubio‐Terres, Alberto García‐Redondo, Joaquı́n Arenas

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Key concepts: Lactic acidosis, Mitochondrial encephalomyopathy, Heteroplasmy, Mitochondrial myopathy, Mitochondrial DNA, Genetics, Myopathy, Mutation

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A mitochondrial tRNALys gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes — Research Paper | ScholarLens