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Journal article

Burden of copy number variation in common variable immunodeficiency

Abstract:
Common variable immunodeficiency (CVID) has been associated recently with a dramatic increase in total copy number variation burden, the cause of which is unclear. In order to explore further the origin and clinical relevance of this finding, we quantified the total genomic copy number variation (CNV) burden in affected patients and evaluated clinical details in relationship to total CNV burden. No correlation was found between total CNV burden and either patient age or time elapsed since symptom onset, and higher total burden did not correlate with incidence of malignancy or other subphenotypes. These findings suggest that the increased CNV burden is static and intrinsic to CVID as a disease. © 2013 British Society for Immunology.

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Publisher copy:
10.1111/cei.12255

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author


Journal:
Clinical and Experimental Immunology More from this journal
Volume:
177
Issue:
1
Pages:
269-271
Publication date:
2014-07-01
DOI:
EISSN:
1365-2249
ISSN:
0009-9104


Language:
English
Keywords:
Pubs id:
pubs:478287
UUID:
uuid:bb535504-e2bb-44ae-a63d-8c6886a9f65f
Local pid:
pubs:478287
Source identifiers:
478287
Deposit date:
2014-08-16

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