Truncating de novo mutations in the Krüppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphisms

BACKGROUND: Krüppel-type zinc finger genes (ZNF) constitute a large yet relatively poorly characterized gene family. ZNF genes encode proteins that recognize specific DNA motifs in gene promotors. They act as transcriptional co-activators or -repressors via interaction with chromatin remodeling prot...

Descripción completa

Detalles Bibliográficos
Autores principales: Stevens, Servi J. C., van Essen, Anthonie J., van Ravenswaaij, Conny M. A., Elias, Abdallah F., Haven, Jaclyn A., Lelieveld, Stefan H., Pfundt, Rolph, Nillesen, Willy M., Yntema, Helger G., van Roozendaal, Kees, Stegmann, Alexander P., Gilissen, Christian, Brunner, Han G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155377/
https://www.ncbi.nlm.nih.gov/pubmed/27964749
http://dx.doi.org/10.1186/s13073-016-0386-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155377/
https://www.ncbi.nlm.nih.gov/pubmed/27964749
http://dx.doi.org/10.1186/s13073-016-0386-9

Ejemplares similares