Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression
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H. Firth | A. Ekici | S. Holder | U. Grasshoff | H. Sticht | M. Zenker | A. Reis | A. Rauch | C. Zweier | E. Wohlleber | H. Engels | A. Gregor | Diana S. Johnson | E. Bijlsma | C. Kraus | M. Zweier | E. Rossier | L. Robertson | Cornelia Kraus | Diana Johnson | H. Firth | S. Holder | Diana S. Johnson