CAGE-defined promoter regions of the genes implicated in Rett Syndrome

BACKGROUND: Mutations in three functionally diverse genes cause Rett Syndrome. Although the functions of Forkhead box G1 (FOXG1), Methyl CpG binding protein 2 (MECP2) and Cyclin-dependent kinase-like 5 (CDKL5) have been studied individually, not much is known about their relation to each other with...

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Detalhes bibliográficos
Publicado no:BMC Genomics
Main Authors: Vitezic, Morana, Bertin, Nicolas, Andersson, Robin, Lipovich, Leonard, Kawaji, Hideya, Lassmann, Timo, Sandelin, Albin, Heutink, Peter, Goldowitz, Dan, Ha, Thomas, Zhang, Peter, Patrizi, Annarita, Fagiolini, Michela, Forrest, Alistair RR, Carninci, Piero, Saxena, Alka
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4522966/
https://ncbi.nlm.nih.gov/pubmed/25539566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-1177
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