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

✍ Scribed by Yolanda Campos; Gustavo Lorenzo; Miguel A Martı́n; Alicia Torregrosa; Pilar del Hoyo; Juan C Rubio; Alberto Garcı́a; Joaquı́n Arenas

No coin nor oath required. For personal study only.

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