Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients

BACKGROUND: More than 85% of Rett syndrome (RTT) patients have heterozygous mutations in the X-linked MECP2 gene which encodes methyl-CpG-binding protein 2, a transcriptional repressor that binds methylated CpG sites. Because MECP2 is subject to X chromosome inactivation (XCI), girls with RTT expres...

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Detalles Bibliográficos
Autores principales: Delgado, Ivan J, Kim, Dong Sun, Thatcher, Karen N, LaSalle, Janine M, Van den Veyver, Ignatia B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1569822/
https://www.ncbi.nlm.nih.gov/pubmed/16859563
http://dx.doi.org/10.1186/1471-2350-7-61

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1569822/
https://www.ncbi.nlm.nih.gov/pubmed/16859563
http://dx.doi.org/10.1186/1471-2350-7-61

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