Phenotype #0000106360

Individual ID 00133613
Associated disease LGMD
Phenotype details -
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD), cardiomyopathy (CM)
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein WB SGCA reduced, SGCG reduced
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-04-18 16:40:26 +02:00 (CEST)
Date last edited 2012-03-09 18:55:42 +01:00 (CET)

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