Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q

Human Genetics

Volumn 118, Issue 6, 2006, Pages 725-729

  Schäffer, Alejandro A ^a   Pfannstiel, Jessica ^b   Webster, A David B ^c   Plebani, Alessandro ^d   Hammarström, Lennart ^e   Grimbacher, Bodo ^b  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b UNIVERSITY OF FREIBURG   (Germany)

^c ROYAL FREE HOSPITAL   (United Kingdom)

^d UNIVERSITY OF BRESCIA   (Italy)

^e KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN A1;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 16Q; CHROMOSOME 6P; CLINICAL ARTICLE; COMMON VARIABLE IMMUNODEFICIENCY; CONTROLLED STUDY; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC IDENTIFICATION; GENETIC LINKAGE; GENOTYPE; HUMAN; IMMUNOGLOBULIN A DEFICIENCY; LINKAGE ANALYSIS; MARKER GENE; PRIORITY JOURNAL; SCORING SYSTEM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; COMMON VARIABLE IMMUNODEFICIENCY; FAMILY; GENETIC LINKAGE; HUMANS; IGA DEFICIENCY; LINKAGE (GENETICS); LOD SCORE;

EID: 32444444461     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-005-0101-1     Document Type: Article

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