MEF2A, myocyte enhancer factor 2A, 4205

N. diseases: 99; N. variants: 14
Disease: Epilepsy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.020 Biomarker disease BEFREE Further, by using unbiased approaches novel neuronal targets of <i>miR-135a</i>, including members of the Mef2 protein family, are identified that begin to explain how deregulation of <i>miR-135a</i> may contribute to epilepsy. 31015341 2019
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.020 GeneticVariation disease BEFREE Several of the MEF2 targets are mutated in human neurological disorders including epilepsy and autism spectrum disorders, suggesting that these disorders may be caused by disruption of an activity-dependent gene program that controls synapse development. 19109909 2008