Global Variome shared LOVD

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Phenotype #0000141889 Individual ID 00179403 Associated disease EE Phenotype details see paper; … Diagnosis/Initial hypomyelination with atrophy basal ganglia and cerebellum (HABC) 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 2018-08-20 21:54:12 +02:00 (CEST) Date last edited N/A

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