Open AccessCorrection: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
Author(s) -
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,
Jun Kwan,
Anthony D. Sandler,
Karin Fuentes Fajardo,
Thomas C. Markello,
Cynthia J. Tifft,
C. Shan Xu,
Elena I. Rugarli,
Thomas Langer,
William A. Gahl,
Camilo Toro
Publication year - 2013
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28
Subject(s) - biology , genetics , ataxia , exome sequencing , mutation , bioinformatics , gene , neuroscience