Global Variome shared LOVD

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Phenotype #0000043034 Individual ID 00056407 Associated disease CMT2 Phenotype details autosomal dominant axonal CMT with early onset, sensory ataxia, tremor, and slow disease progression Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 08y Phenotype/Onset 8y Protein - Owner name Ki Wha Chung Database submission license No license selected Created by Ki Wha Chung Date created 2015-12-24 04:17:24 +01:00 (CET) Date last edited 2016-01-10 06:23:17 +01:00 (CET)

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