The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression

The mechanisms underlying the neurodevelopmental deficits associated with CHARGE syndrome, which include cerebellar hypoplasia, developmental delay, coordination problems, and autistic features, have not been identified. CHARGE syndrome has been associated with mutations in the gene encoding the ATP...

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Detalles Bibliográficos
Autores principales: Whittaker, Danielle E., Riegman, Kimberley L.H., Kasah, Sahrunizam, Mohan, Conor, Yu, Tian, Sala, Blanca Pijuan, Hebaishi, Husam, Caruso, Angela, Marques, Ana Claudia, Michetti, Caterina, Smachetti, María Eugenia Sanz, Shah, Apar, Sabbioni, Mara, Kulhanci, Omer, Tee, Wee-Wei, Reinberg, Danny, Scattoni, Maria Luisa, Volk, Holger, McGonnell, Imelda, Wardle, Fiona C., Fernandes, Cathy, Basson, M. Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330721/
https://www.ncbi.nlm.nih.gov/pubmed/28165338
http://dx.doi.org/10.1172/JCI83408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330721/
https://www.ncbi.nlm.nih.gov/pubmed/28165338
http://dx.doi.org/10.1172/JCI83408

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