Age-related changes in serum immunoglobulins in patients with familial IgA deficiency and common variable immunodeficiency (CVID)

Clinical and Experimental Immunology

Volumn 108, Issue 3, 1997, Pages 477-483

  Johnson, M L ^a,b   Keeton, L G ^a   Zhu, Z B ^a   Volanakis, J E ^a,b   Cooper, M D ^a,b,c,d   Schroeder Jr , H W ^a,b,e  

^a University of Alabama at Birmingham   (United States)

^b University of Alabama at Birmingham   (United States)

^c University of Alabama at Birmingham   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^e The University of Alabama at Birmingham   (United States)

Author keywords

common variable immunodeficiency; genetic basis of disease; hypogammaglobulinaemia; IgA deficiency; MHC haplotype

Indexed keywords

ADOLESCENT; ADULT; AGE; ARTICLE; CHILD; CLINICAL ARTICLE; COMMON VARIABLE IMMUNODEFICIENCY; DIAGNOSTIC VALUE; GENETIC ANALYSIS; HAPLOTYPE; HUMAN; IMMUNOGLOBULIN A DEFICIENCY; IMMUNOGLOBULIN BLOOD LEVEL; MAJOR HISTOCOMPATIBILITY COMPLEX; PATIENT MONITORING; PRIORITY JOURNAL;

EID: 0031006633     PISSN: 00099104     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2249.1997.3801278.x     Document Type: Article

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