Literature DB >> 28278293

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.   

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0167562.].

Entities:  

Year:  2017        PMID： 28278293      PMCID： PMC5344493          DOI： 10.1371/journal.pone.0173719

Source DB:  PubMed          Journal:  PLoS One        ISSN： 1932-6203            Impact factor:   3.240


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.
  1 in total

1.  Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.

Authors:  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
Journal:  PLoS One       Date:  2016-12-09       Impact factor: 3.240
  1 in total

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