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2. Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons. Tao J; Wu H; Sun YE Int Rev Neurobiol; 2009; 89():147-60. PubMed ID: 19900619 [TBL] [Abstract][Full Text] [Related]
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5. MeCP2 and other methyl-CpG binding proteins. Jørgensen HF; Bird A Ment Retard Dev Disabil Res Rev; 2002; 8(2):87-93. PubMed ID: 12112733 [TBL] [Abstract][Full Text] [Related]
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9. MeCP2 in Rett syndrome: transcriptional repressor or chromatin architectural protein? Chadwick LH; Wade PA Curr Opin Genet Dev; 2007 Apr; 17(2):121-5. PubMed ID: 17317146 [TBL] [Abstract][Full Text] [Related]
10. MeCP2 in neurons: closing in on the causes of Rett syndrome. Caballero IM; Hendrich B Hum Mol Genet; 2005 Apr; 14 Spec No 1():R19-26. PubMed ID: 15809268 [TBL] [Abstract][Full Text] [Related]
11. Rett syndrome: a prototypical neurodevelopmental disorder. Neul JL; Zoghbi HY Neuroscientist; 2004 Apr; 10(2):118-28. PubMed ID: 15070486 [TBL] [Abstract][Full Text] [Related]
13. Is Rett syndrome a loss-of-imprinting disorder? Pescucci C; Meloni I; Renieri A Nat Genet; 2005 Jan; 37(1):10-1. PubMed ID: 15624014 [No Abstract] [Full Text] [Related]
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18. No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients. Vourc'h P; Bienvenu T; Beldjord C; Chelly J; Barthélémy C; Müh JP; Andres C Eur J Hum Genet; 2001 Jul; 9(7):556-8. PubMed ID: 11464249 [TBL] [Abstract][Full Text] [Related]
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