Global Variome shared LOVD

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Phenotype #0000172606 Individual ID 00228668 Associated disease BMD Phenotype details see paper; ..., mixed phenotype, delayed motor and mental milestones, elevated creatine kinase (2421 to 5257 U/L) Diagnosis/Initial Becker muscular dystrophy Inheritance Unknown Diagnosis/Definite BMD Age/Examination - Age/Onset - Phenotype/Onset - Age/Diagnosis - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-03-23 20:10:21 +01:00 (CET) Date last edited N/A

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