ATRX links atypical histone methylation recognition mechanisms to human brain function

ATR-X (alpha thalassemia/mental retardation, X-linked) syndrome is a human congenital disorder that causes severe intellectual disabilities. Mutations in the ATRX gene, which encodes an ATP-dependent chromatin-remodeler, are responsible for the syndrome. Approximately 50% of the patient missense mut...

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Detalles Bibliográficos
Autores principales: Iwase, Shigeki, Xiang, Bin, Ghosh, Sharmistha, Ren, Ting, Lewis, Peter W., Cochrane, Jesse C., Allis, C. David, Picketts, David J., Patel, Dinshaw J., Li, Haitao, Shi, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130887/
https://www.ncbi.nlm.nih.gov/pubmed/21666679
http://dx.doi.org/10.1038/nsmb.2062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130887/
https://www.ncbi.nlm.nih.gov/pubmed/21666679
http://dx.doi.org/10.1038/nsmb.2062

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