Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Open Access

Correction

Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

  • Bushra Irum,
  • Shahid Y. Khan,
  • Muhammad Ali,
  • Muhammad Daud,
  • Firoz Kabir,
  • Bushra Rauf,
  • Fareeha Fatima,
  • Hira Iqbal,
  • Arif O. Khan,
  • Saif Al Obaisi,
  • Muhammad Asif Naeem,
  • Idrees A. Nasir,
  • Shaheen N. Khan,
  • Tayyab Husnain,
  • Sheikh Riazuddin,
  • Javed Akram,
  • Allen O. Eghrari,
  •  [ ... ],
  • S. Amer Riazuddin
  • [ view all ]
  • [ view less ]

There are errors in the fourth paragraph of the Results section. The correct paragraph is: To further investigate the possibility of a deletion mutation at the GCNT2 locus in PKCC215, we examined the whole-exome data of three affected individuals, which revealed the absence of variants at chromosome 6 interval harboring GCNT2. A search of variants in proximal and distal regions of GCNT2 identified two SNP’s rs35318586 (chr6: 10,464,803bp) and rs3756954 (chr6: 10,724,327bp) in exome data defining the proximal and distal boundaries of the deletion.

Reference

  1. 1. Irum B, Khan SY, Ali M, Daud M, Kabir F, Rauf B, et al. (2016) Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. PLoS ONE 11(12): e0167562. pmid:27936067

Citation: Irum B, Khan SY, Ali M, Daud M, Kabir F, Rauf B, et al. (2017) Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. PLoS ONE 12(3): e0173719. https://doi.org/10.1371/journal.pone.0173719

Published: March 9, 2017

Copyright: © 2017 Irum 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.