Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. (Q51850375)
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scientific article published in June 2010
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English | Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. |
scientific article published in June 2010 |
Statements
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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. (English)
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Arif B Ekici
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Martin Zenker
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Helen V Firth
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Anita Rauch
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Markus Zweier
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Anne Gregor
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Christiane Zweier
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Hartmut Engels
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Eva Wohlleber
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Emilia K Bijlsma
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Susan E Holder
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Eva Rossier
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Ute Grasshoff
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Diana S Johnson
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Lisa Robertson
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Cornelia Kraus
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1 June 2010
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31
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722-733
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6
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