Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000106676 Individual ID 00133927 Associated disease LGMD2 Inheritance Isolated (sporadic) Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) Age/Examination - Diagnosis/Definite dystrophy, muscular, limb-girdle, type 2C (LGMD-2C) Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details - Protein WB no SGCA, no SGCG Owner name Human Genetics Diagnostic Laboratory - Cochin Hosp J Chelly, F Leturcq Database submission license No license selected Created by Human Genetics Diagnostic Laboratory - Cochin Hosp J Chelly, F Leturcq Date created 2008-10-12 17:35:30 +02:00 (CEST) Date last edited 2012-03-09 18:58:40 +01:00 (CET)

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