Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Sclerosis and ATP8[original query] |
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Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients. Cellular and molecular neurobiology 2007 Sep 27 (6): 695-700. Ahari Solmaz Etemad, Houshmand Massoud, Panahi Mehdi Shafa Shariat, Kasraie Sadaf, Moin Mostafa, Bahar Mohammad A |
Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China. Journal of neurology 2021 Jun . Ni Jie, Liu Zhen, Yuan Yanchun, Li Wanzhen, Hu Yiting, Liu Pan, Hou Xiaorong, Zhu Xiangyu, Tang Xuxiong, Liang Mingyu, Zheng Siqi, Hou Xuan, Du Juan, Tang Jianguang, Jiang Hong, Shen Lu, Tang Beisha, Wang Junli |
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis. PloS one 2022 17 (2): e0263606. Al-Kafaji Ghada, Bakheit Halla F, AlAli Faisal, Fattah Mina, Alhajeri Saad, Alharbi Maram A, Daif Abdulqader, Alsabbagh Manahel Mahmood, Alwehaidah Materah Salem, Bakhiet Mo |
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