Llwytho...
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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Rockefeller University Press
2008
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| Mynediad Ar-lein: | 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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