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

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

Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-02-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3586582
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spelling doaj-5c384d50499a48578c47f2bccbbb1f2a2020-11-25T00:07:12ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-02-019210.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.Tyler Mark PiersonDavid AdamsFlorian BonnPaola MartinelliPraveen F. CherukuriJamie K. TeerNancy F. HansenPedro CruzJames C. MullikinRobert W. BlakesleyGretchen GolasJustin KwanAnthony SandlerKarin Fuentes FajardoThomas MarkelloCynthia TifftCraig BlackstoneElena I. RugarliThomas LangerWilliam A. GahlCamilo Torohttp://europepmc.org/articles/PMC3586582
collection DOAJ
language English
format Article
sources DOAJ
author 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
spellingShingle 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
Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
PLoS Genetics
author_facet 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
author_sort Tyler Mark Pierson
title Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
title_short Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
title_full Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
title_fullStr Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
title_full_unstemmed Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.
title_sort correction: whole-exome sequencing identifies homozygous mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial -aaa proteases.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2013-02-01
url http://europepmc.org/articles/PMC3586582
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