Global Variome shared LOVD

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Phenotype #0000125696 Individual ID 00152961 Associated disease CMS Phenotype details - Diagnosis/Initial syndrome, myasthenic, congenital, slow channel (SCCMS) Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2011-02-13 11:22:31 +01:00 (CET) Date last edited 2013-01-27 10:19:10 +01:00 (CET)

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