Global Variome shared LOVD

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Phenotype #0000116608 Individual ID 00143830 Associated disease ? Diagnosis/Initial congenital myasthenic syndrome (CMS) Diagnosis/Definite CMS-9 Phenotype details see paper; severe congenital myasthenic syndrome Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2015-03-10 00:23:11 +01:00 (CET) Date last edited 2015-03-10 00:23:58 +01:00 (CET)

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