Update on the pathogenesis of hyper IgM syndrome / 国际儿科学杂志
International Journal of Pediatrics
; (6): 10-13, 2013.
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.
Texto completo:
1
Índice:
WPRIM
Tipo de estudio:
Etiology_studies
Idioma:
Zh
Revista:
International Journal of Pediatrics
Año:
2013
Tipo del documento:
Article