Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Mitochondrial Diseases and ND3[original query] |
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Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion 2010 Apr 10 (3): 300-8. Nishigaki Yutaka, Ueno Hitomi, Coku Jorida, Koga Yasutoshi, Fujii Tatsuya, Sahashi Ko, Nakano Kazutoshi, Yoneda Makoto, Nonaka Michiko, Tang Linya, Liou Chia-Wei, Paquis-Flucklinger Veronique, Harigaya Yasuo, Ibi Tohru, Goto Yu-ichi, Hosoya Hiroko, DiMauro Salvatore, Hirano Michio, Tanaka Masas |
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I. BMC pediatrics 2020 1 20 (1): 41. Danhelovska Tereza, Kolarova Hana, Zeman Jiri, Hansikova Hana, Vaneckova Manuela, Lambert Lukas, Kucerova-Vidrova Vendula, Berankova Kamila, Honzik Tomas, Tesarova Marke |
NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia. Current topics in medicinal chemistry 2021 6 21 (11): 938-948. Ivanova Elena Mihailova, Kandilarova Snezhina Mihailova, Lukanov Tzvetelin Ivanov, Naumova Elissaveta Jordanova, Akabalieva Katerina Valentinova, Milanova Vihra Krumo |
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- Page last updated:Apr 29, 2024
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