Browsing by Subject "X-linked agammaglobulinemia"
Now showing items 1-2 of 2
-
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects
(2016-04-02)© 2016 Taylor & Francis. Objectives: Impairment in early B-cell development can cause a predominantly antibody deficiency with severe depletion of peripheral B-cells. Mutations in the gene encoding for Brutons-tyrosine-kinase ... -
Primary antibody deficiency in a tertiary referral hospital: A 30-year experiment
(2015-01-01)© 2015 Esmon Publicidad. Background: Primary antibody deficiency (PAD) is the most common group of primary immunodeficiency disorders (PID), with a broad spectrum of clinical features ranging from severe and recurrent ...