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G.P.18.09 Functional characterisation of a novel mutation causing episodic ataxia type 1 occurring in the KCNA1 gene

✍ Scribed by P. Imbrici; F. Gualandi; M. D’Adamo; P. Cudia; D. De Grandis; A. Ferlini; M. Pessia

No coin nor oath required. For personal study only.

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