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.
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。]
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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.
PLoS One. 2010 Dec 20;5(12):e15687. doi: 10.1371/journal.pone.0015687.
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