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Unusual Presentation of Cerebellar Ataxia Associated with Heterozygous UBA5 and Homozygous CACNA1A Mutations: A Case Report

Eukaryotic Initiation Factor 2B4 Point Mutation Associated with Adult-onset Cerebellar Atrophy and Ataxia

Author:Fletcher, David   Colantonio, Lea   Deng, Yongjia   Frey, Jessica   

Session Name:P6: Movement Disorders: Ataxia 1  

Topic:Movement Disorders  

Program Number:P6.026  

Author Institution: