Global Variome shared LOVD

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Phenotype #0000116602 Individual ID 00143824 Associated disease ? Diagnosis/Initial myasthenic syndrome, congenital (CMS) Diagnosis/Definite CMS-9 Phenotype details - Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Tom Winder Database submission license No license selected Created by Tom Winder Date created 2012-07-03 22:10:33 +02:00 (CEST) Date last edited 2012-07-06 17:49:53 +02:00 (CEST)

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