Gene: MEF2C ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4208
Gene Symbol: MEF2C
MEF2C 		0.010 GeneticVariation disease BEFREE We therefore conclude that the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway. 20513142 2010