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Mitochondrial DNA Part A
DNA Mapping, Sequencing, and Analysis
Volume 27, 2016 - Issue 1
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Original Article

Is mitochondrial tRNASer(UCN) T7501C mutation associated with cardiovascular disease?

Yu DingCentral Laboratory, Hangzhou First People’s Hospital, Hangzhou, China, ;Affiliated Hangzhou Hospital, Nanjing Medical University, Hangzhou, China, and
&
Jinyu HuangAffiliated Hangzhou Hospital, Nanjing Medical University, Hangzhou, China, and ;Department of Cardiology, Hangzhou First People’s Hospital, Hangzhou, ChinaCorrespondence[email protected]
Pages 205-208 | Received 03 Dec 2013, Accepted 05 Jan 2014, Published online: 03 Feb 2014

Citations (4)

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Read on this site (2)

Xue-Jiao Yu & Yu Ding. (2020) The roles of mitochondrial tRNA mutations in non-dystrophic myotonias. Mitochondrial DNA Part B 5:3, pages 3778-3783.
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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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Articles from other publishers (2)

Tian Xia, Ying Pang & Huimin Xiong. (2021) Mutational Screening for Mitochondrial tRNA Mutations in 150 Children with High Myopia. Iranian Journal of Pediatrics 31:5.
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Josef Finsterer, Claudia Stöllberger & Concha Maeztu. (2016) Sudden cardiac death in neuromuscular disorders. International Journal of Cardiology 203, pages 508-515.
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