Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Syndrome and ND3[original query] |
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| Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2007 Feb 96 (2): 211-4. Opdal Siri Hauge, Vege Ashild, Arnestad Marianne, Musse Musse Ahmed, Rognum Torleiv O |
| Mitochondrial DNA associations with East Asian metabolic syndrome. Biochimica et biophysica acta. Bioenergetics 2018 7 1859 (9): 878-892. Chalkia Dimitra, Chang Yi-Cheng, Derbeneva Olga, Lvova Maria, Wang Ping, Mishmar Dan, Liu Xiaogang, Singh Larry N, Chuang Lee-Ming, Wallace Douglas |
| Clinical and molecular characterization of pediatric mitochondrial disorders in south of China. European journal of medical genetics 2020 4 63 (8): 103898. Hu Chaoping, Li Xihua, Zhao Lei, Shi Yiyun, Zhou Shuizhen, Wu Bingbing, Wang |
| 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 |
| Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome. Pediatric neurology 2022 11 138 27-32. Na Ji-Hoon, Lee Young-Mo |
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