Global Variome shared LOVD

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Phenotype #0000125726 Individual ID 00152992 Associated disease CMS Phenotype details phenotype compatible with SCCMS Diagnosis/Initial syndrome, myasthenic, congenital, slow channel (SCCMS) Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Angela Abicht Database submission license No license selected Created by Angela Abicht Date created 2011-12-28 11:54:56 +01:00 (CET) Date last edited 2012-03-09 19:08:25 +01:00 (CET)

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