Global Variome shared LOVD

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Phenotype #0000141924 Individual ID 00179437 Associated disease SCAR Phenotype details see paper; ..., gait instability, speech difficulties, gait and limb ataxia, dysarthria, horizontal nystagmus, cataract; EMG normal Diagnosis/Initial cerebellar ataxia Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-08-21 22:09:59 +02:00 (CEST) Date last edited N/A

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