In the PDF, in the Results section, the second paragraph of subsection "Association study of SNPs and IPH in Han Chinese" was omitted. The paragraph is available below:
Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). Risk of IPH increased 19.0% for each additional risk allele carried (1.190 [1.120-1.263] per allele, p < 0.0001; Figure 2B). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects were not significantly more than that in the control group (ptrend = 0.2752; Figure 2A); and the number of risk alleles did not increase the risk of IFH (1.053 [0.963-1.150] per allele, p = 0.2564; Figure 2C).
Citation: Kong X, Hong J, Chen Y, Chen L, Zhao Z, Li Q, et al. (2013) Correction: Association of Genetic Variants with Isolated Fasting Hyperglycaemia and Isolated Postprandial Hyperglycaemia in a Han Chinese Population. PLoS ONE 8(8): 10.1371/annotation/936a4359-1bf5-4c33-be7d-1468e75eaa8b. https://doi.org/10.1371/annotation/936a4359-1bf5-4c33-be7d-1468e75eaa8b
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Abstract
Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects were not significantly more than that in the control group (ptrend = 0.2752; Figure 2A); and the number of risk alleles did not increase the risk of IFH (1.053 [0.963-1.150] per allele, p = 0.2564; Figure 2C).
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