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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 23, 2012 - Issue 4
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Short Communication

Is mitochondrial tRNALeu(UUR) 3291T>C mutation pathogenic?

Yu Ding;Central Laboratory, Hangzhou First People's Hospital, Hangzhou, People's Republic of China
&
Jianhang Leng;Affiliated Hangzhou Hospital, Nanjing Medical University, Hangzhou, People's Republic of ChinaCorrespondence[email protected]
Pages 323-326 | Received 28 Dec 2011, Accepted 06 Mar 2012, Published online: 03 Apr 2012

Citations (10)

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Read on this site (6)

Yu Ding, Qi Liu, Yao-Shu Teng, Hui Zheng & Jian-Hang Leng. (2019) The mitochondrial tRNAThr G15930A may be a novel mutation associated with hearing impairment. Mitochondrial DNA Part B 4:1, pages 1347-1349.
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Quan-Yong Yi, Gang Deng, Hong-Jian Zhou, Guo-Hai Wu & Luosheng Tang. (2016) Mitochondrial transfer RNA variants and primary congenital glaucoma. Mitochondrial DNA Part A 27:4, pages 2405-2407.
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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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Yu Ding & Jinyu Huang. (2016) Is mitochondrial tRNASer(UCN) T7501C mutation associated with cardiovascular disease?. Mitochondrial DNA Part A 27:1, pages 205-208.
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Qingzhang Zhu, Yuanfeng Zhou, Xiaoping Jin & Xianfang Lin. (2015) The role of mitochondrial tRNAPhe C628T variant in deafness expression. Mitochondrial DNA 26:1, pages 2-6.
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Articles from other publishers (4)

E. Kelland, C.A. Rupar, Asuri N. Prasad, K.Y. Tay, A. Downie & C. Prasad. (2016) The expanding phenotype of MELAS caused by the m.3291T>C mutation in the MT-TL1 gene. Molecular Genetics and Metabolism Reports 6, pages 64-69.
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文玲 汤. (2016) Research Progress on Protective Effects of Polysaccharide on Alcoholic Liver Injury in Mice. Open Journal of Nature Science 04:01, pages 1-7.
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Kaiming Liu, Hui Zhao, Kunqian Ji & Chuanzhu Yan. (2013) MERRF/MELAS overlap syndrome due to the m.3291T>C mutation. Metabolic Brain Disease 29:1, pages 139-144.
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John W. Yarham, Emma L. Blakely, Charlotte L. Alston, Mark E. Roberts, John Ealing, Piyali Pal, Douglass M. Turnbull, Robert McFarland & Robert W. Taylor. (2013) The m.3291T>C mt-tRNALeu(UUR) mutation is definitely pathogenic and causes multisystem mitochondrial disease. Journal of the Neurological Sciences 325:1-2, pages 165-169.
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