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...

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Detalles Bibliográficos
Autores principales: Basson, M. Albert, van Ravenswaaij-Arts, Conny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Trends Journals 2015
Materias:
Review
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

Internet

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

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