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Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complex

✍ Scribed by L.A. Bindoff; M.A. Birch-Machin; L. Farnsworth; D. Gardner-Medwin; J.G. Lindsay; D.M. Turnbull

No coin nor oath required. For personal study only.

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