The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

ATRX syndrome is characterized by X-linked mental retardation associated with α-thalassemia. The gene mutated in this disease, ATRX, encodes a plant homeodomain-like finger and a SWI2/SNF2-like ATPase motif, both of which are often found in chromatin-remodeling enzymes, but ATRX has not been charact...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Xue, Yutong, Gibbons, Richard, Yan, Zhijiang, Yang, Dafeng, McDowell, Tarra L., Sechi, Salvatore, Qin, Jun, Zhou, Sharleen, Higgs, Doug, Wang, Weidong
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 2003
Soggetti:	Biological Sciences
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC196856/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12953102/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.1937626100
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