Global Variome shared LOVD

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Phenotype #0000165479 Individual ID 00217028 Associated disease NEM Phenotype details - Diagnosis/Initial nemaline myopathy Inheritance Unknown Diagnosis/Definite NEM-2 Age/Examination - Age/Diagnosis - Age/Onset <1y Phenotype/Onset - Protein nemaline rods Owner name Tom Winder Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2009-10-23 16:39:07 +02:00 (CEST) Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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