Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C

BACKGROUND: A number of neurodevelopmental syndromes are caused by mutations in genes encoding proteins that normally function in epigenetic regulation. Identification of epigenetic alterations occurring in these disorders could shed light on molecular pathways relevant to neurodevelopment. RESULTS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Grafodatskaya, Daria, Chung, Barian HY, Butcher, Darci T, Turinsky, Andrei L, Goodman, Sarah J, Choufani, Sana, Chen, Yi-An, Lou, Youliang, Zhao, Chunhua, Rajendram, Rageen, Abidi, Fatima E, Skinner, Cindy, Stavropoulos, James, Bondy, Carolyn A, Hamilton, Jill, Wodak, Shoshana, Scherer, Stephen W, Schwartz, Charles E, Weksberg, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573947/
https://www.ncbi.nlm.nih.gov/pubmed/23356856
http://dx.doi.org/10.1186/1755-8794-6-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573947/
https://www.ncbi.nlm.nih.gov/pubmed/23356856
http://dx.doi.org/10.1186/1755-8794-6-1

Ejemplares similares