Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
- PMID: 29155871
- PMCID: PMC5695760
- DOI: 10.1371/journal.pone.0188610
Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0015687.].
Erratum for
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Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes.PLoS One. 2010 Dec 20;5(12):e15687. doi: 10.1371/journal.pone.0015687. PLoS One. 2010. PMID: 21187929 Free PMC article.
References
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- Sadikovic B, Wang J, El-Hattab A, Landsverk M, Douglas G, Brundage EK, et al. (2010) Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes. PLoS ONE 5(12): e15687 https://doi.org/10.1371/journal.pone.0015687 - DOI - PMC - PubMed
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