You have full access to this article via your institution. Thus, our sequence analysis of TNFRSF13B in a large number of cases and controls provides supporting evidence that heterozygous C104R ...
38; 8036 Graz, Austria; [email protected] Background Subtelomeric deletions and duplications may cause syndromic disorders that include features of immunodeficiency. To date, no phenotype of ...
[96] Early diagnosis and appropriate immunoglobulin (Ig) replacement therapy are fundamental for the favorable clinical outcome of common variable immunodeficiency (CVID) patients. Patients with ...