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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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Detaylı Bibliyografya
Asıl Yazarlar: Zentner, Gabriel E., Hurd, Elizabeth A., Schnetz, Michael P., Handoko, Lusy, Wang, Chuanping, Wang, Zhenghe, Wei, Chialin, Tesar, Paul J., Hatzoglou, Maria, Martin, Donna M., Scacheri, Peter C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2010
Konular:
Online Erişim: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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