Rett syndrome: a surprising result of mutation in MECP2

By Dragich Joanna   Houwink-Manville Isa   Schanen Carolyn  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2365-2375

Oxford University Press

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MECP2 mutations account for most cases of typical forms of Rett syndrome

By Bienvenu Thierry   Carrié Alain   de Nicolas  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1377-1384

Oxford University Press

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Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

By Huppke P.   Laccone F.   Krämer N.   Engel W.   Hanefeld F.  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1369-1375

Oxford University Press

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MeCP2 in neurons: closing in on the causes of Rett Syndrome

By Caballero Isabel Martín   Hendrich Brian  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 2089-2089

Oxford University Press

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FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice

By Deng Vivianne   Matagne Valerie   Frerking Matthew   Ohliger Patricia   Budden Sarojini   Pevsner Jonathan   Dissen Gregory A.   Sherman Larry S.   Ojeda Sergio R.  

Human Molecular Genetics, Vol. 16, Iss. 6, 2007-03 ,pp. : 640-650

Oxford University Press

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