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: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population

  • Ciria C. Hernandez,
  • Tara L. Klassen,
  • Laurel G. Jackson,
  • Katharine Gurba,
  • Ningning Hu,
  • Jeffrey L. Noebels,
  • Robert L. Macdonald

In Table 2, three variants corresponding to the GABRP gene were incorrectly described. The R200H variant should be R200H/C, the S293P variant should be R293C, and the R389N variant should be D389N. Please see the corrected Table 2 here.

thumbnail
Download:
Table 2. Unique GABR variants from GECs reported in the 237 ion channel genes project1.

1GECs = genetic epilepsy cases [20]. *GABR variants characterized in this study.

https://doi.org/10.1371/journal.pone.0167264.t001

Reference

  1. 1. Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, et al. (2016) Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. PLoS ONE 11(9): e0162883. pmid:27622563

Citation: Hernandez CC, Klassen TL, Jackson LG, Gurba K, Hu N, Noebels JL, et al. (2016) Correction: Deleterious Rare Variants Reveal Risk for Loss of GABAA Receptor Function in Patients with Genetic Epilepsy and in the General Population. PLoS ONE 11(11): e0167264. https://doi.org/10.1371/journal.pone.0167264

Published: November 21, 2016

Copyright: © 2016 Hernandez 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.