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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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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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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A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation

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American Journal Of Medical Genetics Part A, Vol. 176, Iss. 3, 2018-03 ,pp. : 699-702

John Wiley & Sons Inc

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X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2 −/+ mouse brain

By Braunschweig Daniel   Simcox Thomas   Samaco Rodney C.   LaSalle Janine M.  

Human Molecular Genetics, Vol. 13, Iss. 12, 2004-06 ,pp. : 1275-1286

Oxford University Press

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