Global Variome shared LOVD

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Phenotype #0000067628 Individual ID 00088155 Associated disease Danon;GSD2B Phenotype details see paper; ..., infancy mild hypotonia, global developmental delay, elevated serum CK levels, ... Diagnosis/Initial - Inheritance Familial, X-linked 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 2016-11-18 23:09:50 +01:00 (CET) Date last edited N/A

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