Functional non-synonymous variants of ABCG2 and gout risk

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023728%3A_____%2F17%3AN0000044" target="_blank" >RIV/00023728:_____/17:N0000044 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/17:10364943
Result on the web
<a href="http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=7&SID=C5NrlW3cwcNnLOUTE5Q&page=1&doc=1" target="_blank" >http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=7&SID=C5NrlW3cwcNnLOUTE5Q&page=1&doc=1</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1093/rheumatology/kex295" target="_blank" >10.1093/rheumatology/kex295</a>

Result language
angličtina
Original language name
Functional non-synonymous variants of ABCG2 and gout risk
Original language description
Genetic variants of ABCG2, common and rare, increased the risk of gout. Non-synonymous allelic variants of ABCG2 had a significant effect on earlier onset of gout and the presence of a familial gout history.
Czech name
—
Czech description
—

Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30226 - Rheumatology

Project
<a href="/en/project/NV15-26693A" target="_blank" >NV15-26693A: Function study of allelic variants of urate transporters in primary hyperuricemia and gout</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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