NLE1, notchless homolog 1, 54475

N. diseases: 5; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
0.010 AlteredExpression disease BEFREE Developmental changes in Notch1 and NLE1 expression in a genetic model of absence epilepsy. 28210849 2017