Global Variome shared LOVD

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Phenotype #0000321186 Individual ID 00430389 Associated disease MYOP Phenotype details see paper; ..., myopathy, muscle weakness, hyperCKemia Diagnosis/Initial myopathy Inheritance Familial, autosomal recessive Diagnosis/Definite MMCKR Age/Examination 60y (60 years) 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 2023-01-19 19:57:45 +01:00 (CET) Date last edited N/A

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