Novel dysfunctional variant in ABCG2 as a cause of severe tophaceous gout: biochemical, molecular genetics and functional analysis
Rheumatology (Oxford, England).
2016 Jan ;
55 (1) :
191-4.
[epub] 20150930
Language English Country England, Great Britain Media print-electronic
Document type Letter, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid26428519
PubMed
26428519
DOI
10.1093/rheumatology/kev350
PII: kev350
Knihovny.cz E-resources
- MeSH
- ATP Binding Cassette Transporter, Subfamily G, Member 2 MeSH
- ATP-Binding Cassette Transporters genetics metabolism MeSH
- Gout * genetics metabolism physiopathology MeSH
- Humans MeSH
- Molecular Biology MeSH
- Neoplasm Proteins genetics metabolism MeSH
- Motor Activity physiology MeSH
- Polymorphism, Genetic * MeSH
- Severity of Illness Index MeSH
- Check Tag
- Humans MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- ATP Binding Cassette Transporter, Subfamily G, Member 2 MeSH
- ATP-Binding Cassette Transporters MeSH
- ABCG2 protein, human MeSH Browser
- Neoplasm Proteins MeSH
References provided by Crossref.org
International journal of molecular sciences.
2021 Feb 16 ;
22 (4) :
.
[epub] 20210216
Journal of clinical medicine.
2019 Nov 14 ;
8 (11) :
.
[epub] 20191114
