DiGeorge Syndrome Gene tbx1 Functions through wnt11r to Regulate Heart Looping and Differentiation

DiGeorge syndrome (DGS) is the most common microdeletion syndrome, and is characterized by congenital cardiac, craniofacial and immune system abnormalities. The cardiac defects in DGS patients include conotruncal and ventricular septal defects. Although the etiology of DGS is critically regulated by...

Descripción completa

Detalles Bibliográficos
Autores principales: Choudhry, Priya, Trede, Nikolaus S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606275/
https://www.ncbi.nlm.nih.gov/pubmed/23533583
http://dx.doi.org/10.1371/journal.pone.0058145

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606275/
https://www.ncbi.nlm.nih.gov/pubmed/23533583
http://dx.doi.org/10.1371/journal.pone.0058145

Ejemplares similares