CSNK2B, casein kinase 2 beta, 1460

N. diseases: 34; N. variants: 6
Disease: Myoclonic Epilepsy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014550
Disease: Myoclonic Epilepsy
Myoclonic Epilepsy 		0.010 GeneticVariation disease BEFREE CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy. 28585349 2017