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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Rockefeller University Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2213576/ https://ncbi.nlm.nih.gov/pubmed/18227278 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200706083 |
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