Global Variome shared LOVD

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Phenotype #0000201933 Individual ID 00264089 Associated disease MD Phenotype details see paper; ..., progressive muscle weakness in twenties, prominent exercise-induced myalgia (2/3), distal Miyoshi muscle dystrophy phenotype (2/3)/proximodistal phenotype (1/3) Diagnosis/Initial progressive muscle weakness Inheritance Familial, autosomal recessive Diagnosis/Definite LGMD-2B 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 2019-09-10 19:57:17 +02:00 (CEST) Date last edited N/A

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