Figures
There are a number of errors in the published article.
Reference sequences for genes with identified variants were inadvertently omitted from the published pdf. The GenBank reference sequence records are:
COL1A1 gene: NG_007400.1, COL1A1 mRNA: NM_000088.3
COL1A2 gene: NG_007405.1, COL1A2 mRNA: NM_000089.3
The variant in patient 2, reported as c.2191G>C in Table 2 should be c.2192G>C, which yields the stated amino acid change p.Gly731Ala. Please see the correct Table 2 here.
The variant in patient 4, c.1135G>A, p.Gly379Arg in COL1A2, reported to be in exon 24 actually lies in exon 21.
The variant in patient 7, c.937-3C>T in COL1A2, reported to be in intron 19 actually lies in intron 18.
Sources for the sequence files in S3 Supplementary data information can be found online in the Ensembl database: http://www.ensembl.org/index.html as well as the Osteogenesis Imperfecta Variant Database: https://oi.gene.le.ac.uk/home.php
Reference
Citation: Wang Y, Cui Y, Zhou X, Han J (2015) Correction: Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta. PLoS ONE 10(5): e0127254. https://doi.org/10.1371/journal.pone.0127254
Published: May 1, 2015
Copyright: © 2015 Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited