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Autor:
Cristopher Cardenas-Cruz, Lizeth Jiménez-Santana, Diana E. Campos-Lopez, Celeste Espinoza-Coria, Paola A. Pérez-Correa, Alejandro Mendoza-Arias, Luis D. Mendoza B., M. Edith González S.
Publikováno v:
International Journal of Contemporary Pediatrics.
Background: X-linked agammaglobulinemia (XLA) is a primary immunodeficiency characterized by arrested B cell development, leading to reduced numbers of B lymphocytes and serum immunoglobulin (Ig) levels, due to mutations in the BTK gene located on th