Global Variome shared LOVD

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Phenotype #0000117235 Individual ID 00144498 Associated disease CNM2 Phenotype details centronuclear myopathy; 12y-disease stable Diagnosis/Initial myopathy, centronuclear, autosomal recessive Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 12y (12 years) Age/Diagnosis - Age/Onset - Phenotype/Onset 5y6m Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-11-05 14:02:48 +01:00 (CET) Date last edited 2017-12-15 11:18:36 +01:00 (CET)

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