Global Variome shared LOVD

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Phenotype #0000106693 Individual ID 00133944 Associated disease LGMD Phenotype details - Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD) Inheritance Unknown Diagnosis/Definite LGMD2C Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein IHC partial loss SGC, weak SSPN Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2009-04-29 22:29:53 +02:00 (CEST) Date last edited 2020-10-04 11:07:05 +02:00 (CEST)

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