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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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Dades bibliogràfiques
Publicat a:Proc Natl Acad Sci U S A
Autors principals: Jenness, Christopher, Giunta, Simona, Müller, Manuel M., Kimura, Hiroshi, Muir, Tom W., Funabiki, Hironori
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2018
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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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