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Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation

✍ Scribed by M. Luigetti; G.M. Fabrizi; F. Taioli; A. Conte; A. Del Grande; M. Sabatelli

No coin nor oath required. For personal study only.

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