KCNC3: phenotype, mutations, channel biophysics--a study of 260 familial ataxia patients

Figueroa, Karla P ; Minassian, Natali A ; Stevanin, Giovanni ; Waters, Michael ; Garibyan, Vartan ; Forlani, Sylvie ; Strzelczyk, Adam ; Bürk, Katrin ; Brice, Alexis ; Dürr, Alexandra ; Papazian, Diane M ; Pulst, Stefan M

Human mutation, 2010-02, Vol.31 (2), p.191-196 [Periódico revisado por pares]

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