Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

BACKGROUND: Females with the neurological disorder Rett syndrome are heterozygous for mutations in X-linked MECP2 that encodes methyl-CpG binding protein 2 (MeCP2) thought to act as a transcriptional repressor. To identify target genes for MeCP2 modulation, we studied global gene expression in singl...

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Pubblicato in:	BMC Med Genet
Autori principali:	Traynor, Jeff, Agarwal, Priyanka, Lazzeroni, Laura, Francke, Uta
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2002
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC137585/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12418965/ https://ncbi.nlm.nih.govhttps://doi.org/10.1186/1471-2350-3-12
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