Global Variome shared LOVD

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Phenotype #0000165613 Individual ID 00217162 Associated disease NEM Phenotype details typical NM Diagnosis/Initial nemaline myopathy Inheritance Isolated (sporadic) Diagnosis/Definite NEM-2 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 2014-12-23 14:13:29 +01:00 (CET) Date last edited 2015-02-27 14:55:07 +01:00 (CET)

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