Literature DB >> 22942308

Absence of SLC22A12/URAT1 gene mutations in patients with primary gout.

Rosa J Torres, Eugenio De Miguel, Rebeca Bailen, Juan G Puig.   

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Year:  2012        PMID： 22942308     DOI： 10.3899/jrheum.120451

Source DB:  PubMed          Journal:  J Rheumatol        ISSN： 0315-162X            Impact factor:   4.666


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  3 in total

Review 1.  Genetics of hyperuricemia and gout: implications for the present and future.

Authors:  Ronald L George; Robert T Keenan
Journal:  Curr Rheumatol Rep       Date:  2013-02       Impact factor: 4.592

2.  Complex analysis of urate transporters SLC2A9, SLC22A12 and functional characterization of non-synonymous allelic variants of GLUT9 in the Czech population: no evidence of effect on hyperuricemia and gout.

Authors:  Olha Hurba; Andrea Mancikova; Vladimir Krylov; Marketa Pavlikova; Karel Pavelka; Blanka Stibůrková
Journal:  PLoS One       Date:  2014-09-30       Impact factor: 3.240

3.  The effects of URAT1/SLC22A12 nonfunctional variants, R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression.

Authors:  Masayuki Sakiyama; Hirotaka Matsuo; Seiko Shimizu; Hiroshi Nakashima; Takahiro Nakamura; Akiyoshi Nakayama; Toshihide Higashino; Mariko Naito; Shino Suma; Asahi Hishida; Takahiro Satoh; Yutaka Sakurai; Tappei Takada; Kimiyoshi Ichida; Hiroshi Ooyama; Toru Shimizu; Nariyoshi Shinomiya
Journal:  Sci Rep       Date:  2016-01-29       Impact factor: 4.379
  3 in total

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