Global Variome shared LOVD

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Phenotype #0000163891 Individual ID 00215439 Associated disease LGMD Phenotype details - Diagnosis/Initial dystrophy, muscular, limb-girdle; myopathy Myoshi Inheritance Isolated (sporadic) Diagnosis/Definite LGMD2B Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein IHC DYSF absent Owner name Nicolas Levy Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-12-28 14:43:34 +01:00 (CET) Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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