Loss of ATRX Does Not Confer Susceptibility to Osteoarthritis

The chromatin remodelling protein ATRX is associated with the rare genetic disorder ATR-X syndrome. This syndrome includes developmental delay, cognitive impairment, and a variety of skeletal deformities. ATRX plays a role in several basic chromatin-mediated cellular events including DNA replication...

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Detalles Bibliográficos
Autores principales: Solomon, Lauren A., Russell, Bailey A., Makar, David, Bérubé, Nathalie G., Beier, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875582/
https://www.ncbi.nlm.nih.gov/pubmed/24386478
http://dx.doi.org/10.1371/journal.pone.0085526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875582/
https://www.ncbi.nlm.nih.gov/pubmed/24386478
http://dx.doi.org/10.1371/journal.pone.0085526

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