Global Variome shared LOVD

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Phenotype #0000154703 Individual ID 00206911 Associated disease AOA Diagnosis/Initial ataxia-oculomotor apraxia Diagnosis/Definite AOA-4 Phenotype details see paper; … Inheritance Familial, autosomal recessive 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 2018-11-17 09:15:09 +01:00 (CET) Date last edited N/A

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