Global Variome shared LOVD

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Phenotype #0000128099 Individual ID 00155717 Associated disease ? Diagnosis/Initial neurodegeneration Diagnosis/Definite - Phenotype details see paper; ..., neurodegeneration and cerebellar atrophy Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset 01y Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-03-24 08:27:43 +01:00 (CET) Date last edited N/A

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