Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F16%3A00095912" target="_blank" >RIV/00216224:14110/16:00095912 - isvavai.cz</a>
Alternative codes found
RIV/00159816:_____/16:00065738
Result on the web
<a href="http://dx.doi.org/10.1038/ng.3675" target="_blank" >http://dx.doi.org/10.1038/ng.3675</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/ng.3675" target="_blank" >10.1038/ng.3675</a>
Alternative languages
Result language
angličtina
Original language name
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
Original language description
Selective immunoglobulin A deficiency (IgAD) is the most common primary immunodeficiency in Europeans. Our genome-wide association study (GWAS) meta-analysis of 1,635 patients with IgAD and 4,852 controls identified four new significant (P < 5 × 10-8) loci and association with a rare IFIH1 variant (p.Ile923Val).
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30300 - Health sciences
Result continuities
Project
<a href="/en/project/EF15_003%2F0000469" target="_blank" >EF15_003/0000469: Cetocoen Plus</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Nature Genetics
ISSN
1061-4036
e-ISSN
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Volume of the periodical
48
Issue of the periodical within the volume
11
Country of publishing house
US - UNITED STATES
Number of pages
5
Pages from-to
1425-1429
UT code for WoS article
000386543400020
EID of the result in the Scopus database
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