Common variable immunodeficiency (CVID) in a family: An autosomal dominant mode of inheritance

Netherlands Journal of Medicine

Volumn 59, Issue 3, 2001, Pages 134-139

  Nijenhuis, T ^a   Klasen, I ^a   Weemaes, C M R ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Common variable immunodeficiency; Familial clustering

Indexed keywords

IMMUNOGLOBULIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; B LYMPHOCYTE; CELL COUNT; CELL FUNCTION; CLINICAL ARTICLE; COMMON VARIABLE IMMUNODEFICIENCY; CONTROLLED STUDY; DISEASE COURSE; DYSGAMMAGLOBULINEMIA; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; HUMAN; MALE; PATHOGENESIS; PHENOTYPE; T LYMPHOCYTE;

ADULT; AGAMMAGLOBULINEMIA; AGE OF ONSET; B-LYMPHOCYTES; CHILD, PRESCHOOL; CHROMOSOME MAPPING; COMMON VARIABLE IMMUNODEFICIENCY; DYSGAMMAGLOBULINEMIA; FEMALE; GENES, DOMINANT; HUMANS; IMMUNOGLOBULINS; INFECTION; LYMPHOCYTE COUNT; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; RECURRENCE; RISK FACTORS; T-LYMPHOCYTES;

EID: 0034807747     PISSN: 03002977     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0300-2977(01)00151-6     Document Type: Article

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