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PMID: 3745926 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Molecular analysis of a case of IgA2 deficiency.

Journal of immunogenetics ·Vol. 13 ·No. 1 ·1986-02-00 ·Pages 3-9

Oliviero S, DeMarchi M, Bast BJ, Zegers BJ, van Loghem E, de Lange G, Carbonara O

Abstract

A family with two members with selective IgA2 deficiency was analysed by direct gene analysis with different probes for the IgCH region. No gross gene deletions or rearrangements were detected. Genetic analysis based on serological and molecular markers did not rule out linkage with the IgCH region. However, a defect of other genes not linked to the Ig heavy chain region and controlling the expression of IgA may be possible as well.

MeSH Terms
Dysgammaglobulinemia/genetics,immunology Female Genes Genetic Linkage Humans IgA Deficiency Immunogenetics Immunoglobulin A/genetics Immunoglobulin Allotypes/genetics Mutation Pedigree
Chemicals
Immunoglobulin A Immunoglobulin Allotypes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Oliviero S
DeMarchi M
Bast B J
Zegers B J
van Loghem E
de Lange G
Carbonara O
Article Info
Journal
Journal of immunogenetics
Abbr.
J Immunogenet
ISSN
0305-1811
Published
1986-02-00
Pages
3-9
Language
English
Region
England
NLM ID
0425125
Subset
IM
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