A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway

Cardiofaciocutaneous (CFC) syndrome is a genetic disorder characterized by distinctive facial features, congenital heart defects, and skin abnormalities. Several germline gain-of-function mutations in the RAS/RAF/MEK/ERK pathway are associated with the disease, including KRAS, BRAF, MEK1, and MEK2....

Descripción completa

Detalles Bibliográficos
Autores principales: Popov, Ivan K., Hiatt, Susan M., Whalen, Sandra, Keren, Boris, Ruivenkamp, Claudia, van Haeringen, Arie, Chen, Mei-Jan, Cooper, Gregory M., Korf, Bruce R., Chang, Chenbei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465419/
https://www.ncbi.nlm.nih.gov/pubmed/31024343
http://dx.doi.org/10.3389/fphys.2019.00388

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465419/
https://www.ncbi.nlm.nih.gov/pubmed/31024343
http://dx.doi.org/10.3389/fphys.2019.00388

Ejemplares similares