Multiple common and rare variants of ABCG2 cause gout
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023728%3A_____%2F17%3AN0000062" target="_blank" >RIV/00023728:_____/17:N0000062 - isvavai.cz</a>
Result on the web
<a href="http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=6&SID=D66LlzfkDBAqKPwKpTf&page=1&doc=1" target="_blank" >http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=6&SID=D66LlzfkDBAqKPwKpTf&page=1&doc=1</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1136/rmdopen-2017-000464" target="_blank" >10.1136/rmdopen-2017-000464</a>
Alternative languages
Result language
angličtina
Original language name
Multiple common and rare variants of ABCG2 cause gout
Original language description
We identified 3 common and 19 rare non-synonymous variants of ABCG2. This study revealed that multiple common and rare variants of ABCG2 are independently associated with gout. These results could support both the 'Common Disease, Common Variant' and 'Common Disease, Multiple Rare Variant' hypotheses for the association between ABCG2 and gout susceptibility.
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
30226 - Rheumatology
Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
RMD Open
ISSN
2056-5933
e-ISSN
2056-5933
Volume of the periodical
3
Issue of the periodical within the volume
e000464
Country of publishing house
GB - UNITED KINGDOM
Number of pages
8
Pages from-to
1-8
UT code for WoS article
000443527700007
EID of the result in the Scopus database
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