Research Papers MEF2C Hypofunction in Neuronal and Neuroimmune Populations Produces MEF2C Haploinsufficiency Syndrome–like Behaviors in MiceMutations in MEF2C from the 5q14.3q15 Microdeletion Syndrome Region Are a Frequent Cause of Severe Mental Retardation and Diminish MECP2 and CDKL5 ExpressionComprehensive Investigation of the Phenotype of MEF2C-related disorders in Human Patients: A Systematic ReviewClinical Findings from the Landmark MEF2C-Related Disorders Natural History Studyld. Aberrant Gliogenesis and Excitation in MEF2C Autism Patient hiPSC - Neurons and Cerebral OrganoidsDominant-Interfering forms of MEF2 Generated by Caspase Cleavage Contribute to NMDA-induced Neuronal ApoptosisThe Role of MEF2 Transcription Factor Family in Neuronal Survival and Degeneration
