Citations (8)
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Ying Yang, Taicheng Zhou, Minsheng Peng, Yongying Liu, Yiping Li, Huawei Wang, David M. Irwin & Yaping Zhang. (2016) Complete mtDNA genomes reveal similar penetrances of maternally inherited type 2 diabetes in two Chinese families. Mitochondrial DNA Part A 27:3, pages 2040-2044.
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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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Articles from other publishers (5)
Minhui Xu, Jiji Li, Baoying Guo, Kaida Xu, Yingying Ye & Xiaojun Yan. (2023) Insights into the Deep Phylogeny and Novel Gene Rearrangement of Mytiloidea from Complete Mitochondrial Genome. Biochemical Genetics.
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Siarhei A. Dabravolski, Victoria A. Khotina, Vasily N. Sukhorukov, Vladislav A. Kalmykov, Liudmila M. Mikhaleva & Alexander N. Orekhov. (2022) The Role of Mitochondrial DNA Mutations in Cardiovascular Diseases. International Journal of Molecular Sciences 23:2, pages 952.
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Haochang Hu, Ying Lin, Xiaofeng Xu, Shaoyi Lin, Xiaomin Chen & Shuangshuang Wang. (2020) The alterations of mitochondrial DNA in coronary heart disease. Experimental and Molecular Pathology 114, pages 104412.
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Zoe Daniil, Ourania S. Kotsiou, Alexandros Grammatikopoulos, Sotiria Peletidou, Helen Gkika, Foteini Malli, Katerina Antoniou, Eirini Vasarmidi, Zissis Mamuris, Konstantinos Gourgoulianis & Emily Zifa. (2018) Detection of mitochondrial transfer RNA (mt-tRNA) gene mutations in patients with idiopathic pulmonary fibrosis and sarcoidosis. Mitochondrion 43, pages 43-52.
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Rogério Marins Alves, Sueli Matilde da Silva Costa, Paulo Mauricio do Amôr Divino Miranda, Priscila Zonzini Ramos, Thiago Gibbin Marconi, Gisele Santos Oliveira, Arthur Menino Castilho & Edi Lúcia Sartorato. (2016) Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry. BMC Medical Genetics 17:1.
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