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

  • Pierson T
  • Adams D
  • Bonn F
  • et al.
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Abstract

[This corrects the article on p. e1002325 in vol. 7.].

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APA

Pierson, T. M., Adams, D., Bonn, F., Martinelli, P., Cherukuri, P. F., Teer, J. K., … Toro, C. (2013). Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases. PLoS Genetics, 9(2). https://doi.org/10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28

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