Global Variome shared LOVD

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Phenotype #0000170711 Individual ID 00225599 Associated disease LGMD Phenotype details see paper; ..., CK level normal; 37y-loss of ambulation; 46y-no cardiac/respiratory complications Diagnosis/Initial limb-girdle muscular dystrophy Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 09y 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 2019-02-18 19:47:26 +01:00 (CET) Date last edited N/A

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