Author(s): Jorge, A ; Melancia, D ; Figueiredo, C ; Galego, O ; Oliveira, J ; Martins, AI ; Lemos, J
Date: 2022
Persistent ID: http://hdl.handle.net/10400.17/4505
Origin: Repositório do Centro Hospitalar de Lisboa Central, EPE
Subject(s): Ataxia / complications; Ataxia / genetics; Humans; Kv1.1 Potassium Channel / genetics; Mutation / genetics; Myokymia*; Nystagmus, Pathologic* / genetics; HSAC NEU
