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Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome
CHARGE syndrome is a rare genetic syndrome characterised by a unique combination of multiple organ anomalies. Dominant loss-of-function mutations in the gene encoding chromodomain helicase DNA binding protein 7 (CHD7), which is an ATP-dependent chromatin remodeller, have been identified as the cause...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier Trends Journals
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604214/ https://www.ncbi.nlm.nih.gov/pubmed/26411921 http://dx.doi.org/10.1016/j.tig.2015.05.009 |