Gene: SCN8A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A 		0.300 GermlineCausalMutation disease ORPHANET Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation. 26677014 2016