Gene: DCX ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1641
Gene Symbol: DCX
DCX 		0.010 GeneticVariation disease BEFREE Mutations of the DCX gene (Xp22.3) cause X-linked lissencephaly in males and double cortex syndrome (DCS) or subcortical band heterotopia (SBH) in females. 19619967 2010