Global Variome shared LOVD

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Phenotype #0000155813 Individual ID 00208044 Associated disease MYOP Phenotype details myopathy, cardiomyopathy, restrictive, atrioventricular block Diagnosis/Initial desmin related myopathy Inheritance Familial, autosomal recessive Diagnosis/Definite MFM-1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein DES aggregates Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2008-06-20 20:39:37 +02:00 (CEST) Date last edited 2018-12-07 14:14:59 +01:00 (CET)

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