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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| Description | scientific article published in June 2010 |
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author: Martin Zenker Arif B. Ekici André Reis Helen Firth Heinrich Sticht Anita Rauch |
| Publication date | June 1, 2010 |
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