Global Variome shared LOVD

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Phenotype #0000302452 Individual ID 00410348 Associated disease HARP Phenotype details - Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite pantothenate kinase associated neurodegeneration Age/Examination - Age/Diagnosis 07y Age/Onset 01y Phenotype/Onset gait dystonia Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-05-24 14:37:58 +02:00 (CEST) Date last edited 2022-05-24 14:57:24 +02:00 (CEST)

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