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The m.5650G > A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy

✍ Scribed by Robert McFarland; Helen Swalwell; Emma L. Blakely; Langping He; Emma J. Groen; Douglass M. Turnbull; Kate M. Bushby; Robert W. Taylor

No coin nor oath required. For personal study only.

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The m.5650G&#xa0;>&#xa0;A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy