LRBA in the endomembrane system

ABSTRACT: Bi-allelic mutations in LRBA (from Lipopolysaccharide-responsive and beige-like anchor protein) result in a primary immunodeficiency with clinical features ranging from hypogammaglobulinemia and lymphoproliferative syndrome to inflammatory bowel disease and heterogeneous autoimmune manifes...

Full description

Autores:

Martínez Jaramillo, Catalina
Trujillo Vargas, Claudia Milena

Tipo de recurso:

Article of investigation

Fecha de publicación:

2018

Institución:

Universidad de Antioquia

Repositorio:

Repositorio UdeA

Idioma:

eng

OAI Identifier:

oai:bibliotecadigital.udea.edu.co:10495/23007

Acceso en línea:

http://hdl.handle.net/10495/23007
https://colombiamedica.univalle.edu.co/index.php/comedica/article/view/3911

Palabra clave:

Autofagia
Autophagy
Apoptosis
Apoptosis
Primary immunodeficiencies
LRBA deficiency
Inmunodeficiencias primarias
Deficiencia de LRBA
Vesicle trafficking
Tráfico vesicular

Rights

openAccess

License

http://creativecommons.org/licenses/by-nc-nd/2.5/co/