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Mutations in MEF2C from the 5q14.3q15 Microdeletion Syndrome Region Are a Frequent Cause of Severe Mental Retardation and Diminish MECP2 and CDKL5 Expression
- All authors
- Zweier, M.; Gregor, A.; Zweier, C.; Engels, H.; Sticht, H.; Wohlleber, E.; Bijlsma, E.K.; Holder, S.E.; Zenker, M.; Rossier, E.; Grasshoff, U.; Johnson, D.S.; Robertson, L.; Firth, H.V.; Kraus, C.; Ekici, A.B.; Reis, A.; Rauch, A.
- Date
- 2010-06-30
- Journal
- Human Mutation
- Volume
- 31
- Issue
- 6
- Pages
- 722 - 733