Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57582
Gene Symbol: KCNT1
KCNT1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.010 GeneticVariation BEFREE We identified a novel de novo KCNT1 variant in a patient with early-infantile epileptic encephalopathy (EIEE) and status dystonicus, a life-threatening movement disorder. 31560846

2019