Global Variome shared LOVD

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Phenotype #0000067630 Individual ID 00088157 Associated disease Danon;GSD2B Phenotype details see paper; ..., presented with HCM, Wolff-Parkinson-White syndrome, skeletal myopathy as teenager; carrier mother developed DCM during 40s, ... Diagnosis/Initial - Inheritance Familial, X-linked dominant Diagnosis/Definite - 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 2016-11-19 18:55:52 +01:00 (CET) Date last edited N/A

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