Global Variome shared LOVD

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Phenotype #0000162315 Individual ID 00213863 Associated disease LGMD Phenotype details proximal muscle weakness lower extremity, involvement proximal muscles upper limb shoulder girdle; serum CK 901 U/L Diagnosis/Initial limb-girdle muscular dystrophy Inheritance Familial, autosomal recessive Diagnosis/Definite LGMD2A Age/Examination - Age/Diagnosis - Age/Onset 59y Phenotype/Onset - Protein - Owner name Ieke Ginjaar Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-08-17 16:04:08 +02:00 (CEST) Date last edited 2020-10-06 14:48:05 +02:00 (CEST)

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