Associated Papers
MEF2C Hypofunction in Neuronal and Neuroimmune Populations Produces MEF2C Haploinsufficiency Syndrome-like Behaviors in Mice.
Harrington AJ et al.
Biological Psychiatry, 2020
MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
Yuan F et al.
Clinical Chemistry and Laboratory Medicine, 2018
MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review.
Rocha H et al.
European Journal of Medical Genetics, 2016
Microdeletion 5q14.3 and anomalies of brain development.
Hotz A et al.
American Journal of Medical Genetics. Part A, 2013
Refining the phenotype associated with MEF2C point mutations.
Bienvenu T et al.
Neurogenetics, 2013
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression.
Zweier M et al.
Human Mutation, 2010
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