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Correction

Correction: Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?

Stephen Eyre*, John Bowes, Catherine Potter, Jane Worthington and Anne Barton

Author Affiliations

ARC-EU, University of Manchester, UK

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Arthritis Research & Therapy 2008, 10:405  doi:10.1186/ar2469


See related research by Eyre et al., http://arthritis-research.com/content/8/4/R117


The electronic version of this article is the complete one and can be found online at: http://arthritis-research.com/content/10/4/405


Published:8 August 2008

© 2008 BioMed Central Ltd

Correction

Following publication of our article [1] we have noticed the following error in nomenclature: All four polymorphisms studied were referred to as FCRL3-169*C/T.

FCRL3-169*C/T (fclr3_3, rs7528684) is correctly named.

FCRL3-169*C/T (fclr3_4, rs11264799) should be FCRL3-110*C/T (fclr3_4, rs11264799).

FCRL3-169*C/T (fclr3_5, rs945635) should be FCRL3+358*C/G (fclr3_5, rs945635).

FCRL3-169*C/T (fclr3_6, rs3761959) should be FCRL3+1370*A/G (fclr3_6, rs3761959).

Thus, Table 1 should appear as shown.

Table 1. Genotype frequencies of Fc receptor-like 3 (FCRL3) single nucleotide polymorphisms in rheumatoid arthritis cases, in controls and in subgroups

Within 'Patients and methods', the paragraph 'Polymorphisms selected' should read as follows:

Four SNPs – FCRL3-169*C/T (fclr3_3, rs7528684), FCRL3-110*C/T (fclr3_4, rs11264799), FCRL3+358*C/G (fclr3_5, rs945635) and FCRL3+1370*A/G (fclr3_6, rs3761959) – were initially selected for investigation because they had all been associated with RA in the Japanese population on single-point analysis, because the SNPs formed a haplotype associated with RA and because the most probable disease causal SNP (FCRL3-169*C/T (fclr3_3, rs7528684)) was included [7].

The second paragraph of 'Results' should read as follows:

No deviation from Hardy–Weinberg expectations was observed for any of the SNPs in either cases or controls. Interim analysis after genotyping a subset of the total cohort revealed that extensive linkage disequilibrium was present across the four SNPs tested. Indeed, the D' value between all the SNPs was 0.98 while the correlation between SNPs FCRL3-169*C/T (fclr3_3, rs7528684), FCRL3+358*C/G fclr3_5 (rs945635) and FCRL3+1370*A/G fclr3_6 (rs3761959) was also 0.98 in this sample. The correlation between these SNPs and FCRL3-110*C/T fclr3_4 (rs11264799) was 0.6 or greater, reflecting the difference in allele frequency of this SNP compared with the others. Hence, genotyping of all four SNPs was unnecessary and, in the remaining samples, only the putative disease causal polymorphism was genotyped.

The above changes in no way affect the conclusions of the study.

Competing interests

The authors declare that they have no competing interests.

References

  1. Eyre S, Bowes J, Potter C, Worthington J, Barton A: Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?

    Arthritis Research & Therapy 2006, 8:R117. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL