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CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis
De novo mutation of the gene encoding chromodomain helicase DNA-binding protein 7 (CHD7) is the primary cause of CHARGE syndrome, a complex developmental disorder characterized by the co-occurrence of a specific set of birth defects. Recent studies indicate that CHD7 functions as a transcriptional r...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2928125/ https://ncbi.nlm.nih.gov/pubmed/20591827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq265 |
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