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1
Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes.更正：线粒体DNA缺失综合征断点处的序列同源性与临床表型
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2
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本文引用的文献

1
Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes.线粒体 DNA 缺失综合征的断裂点序列同源性和临床表型。
PLoS One. 2010 Dec 20;5(12):e15687. doi: 10.1371/journal.pone.0015687.

更正：线粒体DNA缺失综合征断点处的序列同源性与临床表型

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes.

作者信息

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

出版信息

PLoS One. 2017 Nov 20;12(11):e0188610. doi: 10.1371/journal.pone.0188610. eCollection 2017.

DOI:10.1371/journal.pone.0188610
PMID:29155871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5695760/
Abstract

[This corrects the article DOI: 10.1371/journal.pone.0015687.].

摘要

[本文更正了文章的数字对象标识符：10.1371/journal.pone.0015687。]