Loss of ATRX leads to chromosome cohesion and congression defects

αThalassemia/mental retardation X linked (ATRX) is a switch/sucrose nonfermenting-type ATPase localized at pericentromeric heterochromatin in mouse and human cells. Human ATRX mutations give rise to mental retardation syndromes characterized by developmental delay, facial dysmorphisms, cognitive def...

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Detalles Bibliográficos
Autores principales: Ritchie, Kieran, Seah, Claudia, Moulin, Jana, Isaac, Christian, Dick, Frederick, Bérubé, Nathalie G.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213576/
https://www.ncbi.nlm.nih.gov/pubmed/18227278
http://dx.doi.org/10.1083/jcb.200706083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213576/
https://www.ncbi.nlm.nih.gov/pubmed/18227278
http://dx.doi.org/10.1083/jcb.200706083

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