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Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development
GTF2I and GTF2IRD1 encoding the multifunctional transcription factors TFII-I and BEN are clustered at the 7q11.23 region hemizygously deleted in Williams-Beuren syndrome (WBS), a complex multisystemic neurodevelopmental disorder. Although the biochemical properties of TFII-I family transcription fac...
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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2629217/ https://ncbi.nlm.nih.gov/pubmed/19109438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0811531106 |
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