Gene: CUX2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23316
Gene Symbol: CUX2
CUX2 		0.300 GermlineCausalMutation disease ORPHANET The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. 29630738 2018