Your browser doesn't support javascript.
loading
Update on the pathogenesis of hyper IgM syndrome / 国际儿科学杂志
Article en Zh | WPRIM | ID: wpr-430185
Biblioteca responsable: WPRO
ABSTRACT
The hyper immunoglobulin M syndromes(HIGM) are a heterogeneous group of genetic disorders resulting in defects of immunoglobulin class switch recombination,with or without defects of somatic hypermutation.They can be classified as defects of signalling through CD40 causing combined immunodeficiency,or intrinsic defects in B cells of the mechanism of class switch recombination resulting in a pure humoral immunodeficiency.This review summarizes the molecular pathogenesis of HIGM.
Palabras clave
Texto completo: 1 Índice: WPRIM Tipo de estudio: Etiology_studies Idioma: Zh Revista: International Journal of Pediatrics Año: 2013 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudio: Etiology_studies Idioma: Zh Revista: International Journal of Pediatrics Año: 2013 Tipo del documento: Article