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author Pierson, Tyler Mark
Adams, David
Bonn, Florian
Martinelli, Paola
Cherukuri, Praveen F.
Teer, Jamie K.
Hansen, Nancy F.
Cruz, Pedro
Mullikin, James C.
Blakesley, Robert W.
Golas, Gretchen
Kwan, Justin
Sandler, Anthony
Fuentes Fajardo, Karin
Markello, Thomas
Tifft, Cynthia
Blackstone, Craig
Rugarli, Elena I.
Langer, Thomas
Gahl, William A.
Toro, Camilo
author_facet Pierson, Tyler Mark
Adams, David
Bonn, Florian
Martinelli, Paola
Cherukuri, Praveen F.
Teer, Jamie K.
Hansen, Nancy F.
Cruz, Pedro
Mullikin, James C.
Blakesley, Robert W.
Golas, Gretchen
Kwan, Justin
Sandler, Anthony
Fuentes Fajardo, Karin
Markello, Thomas
Tifft, Cynthia
Blackstone, Craig
Rugarli, Elena I.
Langer, Thomas
Gahl, William A.
Toro, Camilo
author_sort Pierson, Tyler Mark
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spelling pubmed-35865822013-03-04 Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases Pierson, Tyler Mark Adams, David Bonn, Florian Martinelli, Paola Cherukuri, Praveen F. Teer, Jamie K. Hansen, Nancy F. Cruz, Pedro Mullikin, James C. Blakesley, Robert W. Golas, Gretchen Kwan, Justin Sandler, Anthony Fuentes Fajardo, Karin Markello, Thomas Tifft, Cynthia Blackstone, Craig Rugarli, Elena I. Langer, Thomas Gahl, William A. Toro, Camilo PLoS Genet Correction Public Library of Science 2013-02-27 /pmc/articles/PMC3586582/ http://dx.doi.org/10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28 Text en © 2013 Public Library of Science http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Correction
Pierson, Tyler Mark
Adams, David
Bonn, Florian
Martinelli, Paola
Cherukuri, Praveen F.
Teer, Jamie K.
Hansen, Nancy F.
Cruz, Pedro
Mullikin, James C.
Blakesley, Robert W.
Golas, Gretchen
Kwan, Justin
Sandler, Anthony
Fuentes Fajardo, Karin
Markello, Thomas
Tifft, Cynthia
Blackstone, Craig
Rugarli, Elena I.
Langer, Thomas
Gahl, William A.
Toro, Camilo
Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title_full Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title_fullStr Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title_full_unstemmed Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title_short Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
title_sort correction: whole-exome sequencing identifies homozygous afg3l2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-aaa proteases
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586582/
http://dx.doi.org/10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28
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