Global Variome shared LOVD

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Phenotype #0000203901 Individual ID 00266121 Associated disease SPG Phenotype details see paper; ..., late teens gait ataxia, spasticity, dysphagia; Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite SPG-76 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 2019-10-14 08:17:51 +02:00 (CEST) Date last edited N/A

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