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Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695760/ https://www.ncbi.nlm.nih.gov/pubmed/29155871 http://dx.doi.org/10.1371/journal.pone.0188610 |
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author | Sadikovic, Bekim Wang, Jing El-Hattab, Ayman W. Landsverk, Megan Douglas, Ganka Brundage, Ellen K. Craigen, William J. Schmitt, Eric S. Wong, Lee-Jun C. |
author_facet | Sadikovic, Bekim Wang, Jing El-Hattab, Ayman W. Landsverk, Megan Douglas, Ganka Brundage, Ellen K. Craigen, William J. Schmitt, Eric S. Wong, Lee-Jun C. |
author_sort | Sadikovic, Bekim |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5695760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56957602017-11-30 Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes Sadikovic, Bekim Wang, Jing El-Hattab, Ayman W. Landsverk, Megan Douglas, Ganka Brundage, Ellen K. Craigen, William J. Schmitt, Eric S. Wong, Lee-Jun C. PLoS One Correction Public Library of Science 2017-11-20 /pmc/articles/PMC5695760/ /pubmed/29155871 http://dx.doi.org/10.1371/journal.pone.0188610 Text en © 2017 Sadikovic et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Correction Sadikovic, Bekim Wang, Jing El-Hattab, Ayman W. Landsverk, Megan Douglas, Ganka Brundage, Ellen K. Craigen, William J. Schmitt, Eric S. Wong, Lee-Jun C. Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title | Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title_full | Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title_fullStr | Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title_full_unstemmed | Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title_short | Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes |
title_sort | correction: sequence homology at the breakpoint and clinical phenotype of mitochondrial dna deletion syndromes |
topic | Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695760/ https://www.ncbi.nlm.nih.gov/pubmed/29155871 http://dx.doi.org/10.1371/journal.pone.0188610 |
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