Gene: CACNB4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 785
Gene Symbol: CACNB4
CACNB4 		0.010 GeneticVariation disease BEFREE A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. 18755274 2008