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Correction

Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

  • Tyler Mark Pierson,
  • David Adams,
  • Florian Bonn,
  • Paola Martinelli,
  • Praveen F. Cherukuri,
  • Jamie K. Teer,
  • Nancy F. Hansen,
  • Pedro Cruz,
  • James C. Mullikin,
  • Robert W. Blakesley,
  • Gretchen Golas,
  • Justin Kwan,
  • Anthony Sandler,
  • Karin Fuentes Fajardo,
  • Thomas Markello,
  • Cynthia Tifft,
  • Craig Blackstone,
  • Elena I. Rugarli,
  • Thomas Langer,
  • William A. Gahl,
  •  [ ... ],
  • Camilo Toro
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The XML annotation for the name of the 9th author, James C. Mullikin, is incorrect. The correct annotation should indicate that this author's surname is "Mullikin" rather than "Mullikin for the NISC Comparative Sequencing Program".

Citation: Pierson TM, Adams D, Bonn F, Martinelli P, Cherukuri PF, Teer JK, et al. (2013) Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases. PLoS Genet 9(2): 10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28. https://doi.org/10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28

Published: February 27, 2013

Copyright: © 2013 . 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.

Competing interests: No competing interests declared.