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

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Detalles Bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2013
Assuntos:
Correction
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3586582/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28
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