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HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome
Mutations in CDCA7, the SNF2 family protein HELLS (LSH), or the DNA methyltransferase DNMT3b cause immunodeficiency–centromeric instability–facial anomalies (ICF) syndrome. While it has been speculated that DNA methylation defects cause this disease, little is known about the molecular function of C...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5798369/ https://ncbi.nlm.nih.gov/pubmed/29339483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1717509115 |
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