Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000135718 Individual ID 00168055 Associated disease ataxia Diagnosis/Initial - Diagnosis/Definite - Phenotype details Cerebellar ataxia, Gait and Reading difficulties, Dysarthria, LL & UL ataxia, Mild cerebellar atrophy Inheritance Familial, autosomal recessive Age/Examination - Age/Onset 39y Phenotype/Onset - Protein - Owner name Inge Meijer Database submission license No license selected Created by Inge Meijer Date created 2018-07-26 22:41:26 +02:00 (CEST) Date last edited N/A

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