Cargando...
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...
Guardado en:
| Publicado en: | Trends Genet |
|---|---|
| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier Trends Journals
2015
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4604214/ https://ncbi.nlm.nih.gov/pubmed/26411921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2015.05.009 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|