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Open Access

Correction

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

  • Zafar Iqbal,
  • Siri L. Rydning,
  • Iselin M. Wedding,
  • Jeanette Koht,
  • Lasse Pihlstrøm,
  • Aina H. Rengmark,
  • Sandra P. Henriksen,
  • Chantal M. E. Tallaksen,
  • Mathias Toft

The last four lines are missing from the legend for Table 3. Please see the complete legend and table here.

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Table 3. List of variants of uncertain significance.

https://doi.org/10.1371/journal.pone.0186571.t001

Reference

  1. 1. Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, et al. (2017) Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia. PLoS ONE 12(3): e0174667. https://doi.org/10.1371/journal.pone.0174667. pmid:28362824

Citation: Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, et al. (2017) Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia. PLoS ONE 12(10): e0186571. https://doi.org/10.1371/journal.pone.0186571

Published: October 12, 2017

Copyright: © 2017 Iqbal 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.