Global Variome shared LOVD

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Phenotype #0000106611 Individual ID 00133862 Associated disease LGMD Phenotype details - Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD) Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 7y Phenotype/Onset - Protein WB SGCA 5%, IHC SGCA, SGCD reduced, SGCB severely reduced, SGCG absent Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-07-13 16:38:45 +02:00 (CEST) Date last edited 2012-03-09 19:39:00 +01:00 (CET)

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