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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 26, 2015 - Issue 2
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Short Communication

Is mitochondrial tRNACys G5821A a deleterious mutation?

Lijuan WeiThe First Affiliated Hospital of Henan University of Science and Technology, Luoyang, ChinaCorrespondence[email protected]
,
Wengen GaoThe First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
,
Yafei MaThe First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
,
Quanxing CaoThe First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
&
Xianfen ZhangThe First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
Pages 202-204 | Received 06 Jan 2014, Accepted 25 Jan 2014, Published online: 12 Mar 2014

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Read on this site (2)

Jifa Zhu, Xiao Zhang & Ling Li. (2016) Transition of 1628C > T in mitochondrial tRNAVal gene should not be regarded as a mutation associated with hypertrophic cardiomyopathy. Mitochondrial DNA Part A 27:2, pages 1340-1342.
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Zhiyi Luo. (2016) Mitochondrial tRNAArg T10454C variant may not influence the clinical expression of deafness associated 12S rRNA A1555G mutation. Mitochondrial DNA Part A 27:2, pages 1137-1140.
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Articles from other publishers (1)

Iman Ibrahim, Mev Dominguez-Valentin, Bernard Segal, Anthony Zeitouni & Sabrina Daniela da Silva. (2018) Mitochondrial mutations associated with hearing and balance disorders. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 810, pages 39-44.
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