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Correction: Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta

  • Yao Wang,
  • Yazhou Cui,
  • Xiaoyan Zhou,
  • Jinxiang Han
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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

  1. 1. Wang Y, Cui Y, Zhou X, Han J (2015) Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta. PLoS ONE 10(3): e0119553. pmid:25742658