Global Variome shared LOVD

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Phenotype #0000162314 Individual ID 00213862 Associated disease hCK Phenotype details asymptomatic Diagnosis/Initial hCK, limb-girdle muscular dystrophy Inheritance Unknown Diagnosis/Definite hCK Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein WB CAPN3 5% Owner name Marina Fanin 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 2013-02-01 19:44:08 +01:00 (CET)

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