Skip to content


You're viewing the new version of our site. Please leave us feedback.

Learn more

BMC Medical Genetics

Open Access

Erratum to: Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case–control study

  • Zhao-Wei Zhou1, 2,
  • Ling-Ling Cui1, 2,
  • Lin Han1, 2,
  • Can Wang1, 2,
  • Zhi-Jian Song3,
  • Jia-Wei Shen3,
  • Zhi-Qiang Li3,
  • Jian-Hua Chen3,
  • Zu-Jia Wen3,
  • Xiao-Min Wang1, 2,
  • Yong-Yong Shi3Email author and
  • Chang-Gui Li1, 2Email author
BMC Medical Genetics201516:99

Published: 28 October 2015

The original article was published in BMC Medical Genetics 2015 16:66


Unfortunately the original version of this article [1] contained a mistake. It came to the authors’ attention that the corresponding authors of the article were not listed correctly, an error which arose during production. Both Yong-Yong Shi ( and Chang-Gui Li ( should have been listed as joint corresponding authors.

The full author list should read:

Zhao-Wei Zhou1,2, Ling-Ling Cui1,2, Lin Han1,2, Can Wang1,2, Zhi-Jian Song3, Jia-Wei Shen3, Zhi-Qiang Li3, Jian-Hua Chen3, Zu-Jia Wen3, Xiao-Min Wang1,2, Yong-Yong Shi3*and Chang-Gui Li1,2*

*Corresponding authors: Chang-Gui Li and Yong-Yong Shi



Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

Shandong Gout Clinical Medical Center, The Affiliated Hospital of Qingdao University
Shandong Provincial Key Laboratory of Metabolic Disease, The Affiliated Hospital of Qingdao University
Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University


  1. Zhou ZW et al. Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study. BMC Med Genet. 2015;16:66.View ArticlePubMedPubMed CentralGoogle Scholar


© Zhou et al. 2015