Global Variome shared LOVD

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Phenotype #0000045738 Individual ID 00059232 Associated disease SPG11 Phenotype details spastic paraplegia, muscle wasting, ataxia, dysarthria, hypokinesia, rigidity Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 23y (23 years) Age/Diagnosis - Age/Onset 13y Phenotype/Onset spastic paraplegia Protein - Owner name Mahmoud Koko Database submission license No license selected Created by Mahmoud Koko Date created 2016-03-04 11:15:37 +01:00 (CET) Date last edited 2016-03-18 16:19:43 +01:00 (CET)

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