Global Variome shared LOVD

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Phenotype #0000125722 Individual ID 00152987 Associated disease CMS Phenotype details - Diagnosis/Initial syndrome, myasthenic, congenital, slow channel Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 1d Phenotype/Onset decreased movements in utero, weak cry and feeble suck 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 11:28:19 +01:00 (CET) Date last edited 2012-12-21 10:13:06 +01:00 (CET)

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