Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Syndrome and LHON[original query] |
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| Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001. Internal medicine journal 0 34 (1-2): 10-9. Marotta R, Chin J, Quigley A, Katsabanis S, Kapsa R, Byrne E, Collins |
| Leber hereditary optic neuropathy: do folate pathway gene alterations influence the expression of mitochondrial DNA mutation? Iranian journal of public health 2012 11 39 (3): 53-60. Aleyasin A, Ghazanfari M, Houshmand |
| Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for OPA1/OPA3/LHON. Neuro-ophthalmology (Aeolus Press) 2018 3 42 (2): 73-82. Galvez-Ruiz Alberto, Galindo-Ferreiro Alicia, Schatz Patr |
| 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 |
| Leber's hereditary optic neuropathy companied with multiple-related diseases. Frontiers in human neuroscience 2022 11 16 964550. Sun Ming-Ming, Zhou Huan-Fen, Sun Qiao, Li Hong-En, Liu Hong-Juan, Song Hong-Lu, Yang Mo, Teng Da, Wei Shi-Hui, Xu Quan-Ga |
- Page last reviewed:Feb 1, 2024
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