| Literature DB >> 21386793 |
Abstract
OA is not a disease in short supply of phenotypic definitions. Indeed, numerous classification options complicate the design of genetic studies seeking associations within the obscuring array of heterogeneity. New recommendations offer some progress toward clarifying OA definitions, but much-needed guidelines are wanting.Entities:
Mesh:
Year: 2011 PMID: 21386793 DOI: 10.1038/nrrheum.2011.26
Source DB: PubMed Journal: Nat Rev Rheumatol ISSN: 1759-4790 Impact factor: 20.543