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Page last updated: 2024-08-17

rotenone and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

rotenone has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Oley, CA; Parker, WD; Parks, JK1

Other Studies

1 other study(ies) available for rotenone and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

ArticleYear
A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.
    The New England journal of medicine, 1989, May-18, Volume: 320, Issue:20

    Topics: Electron Transport; Hereditary Sensory and Motor Neuropathy; Humans; Male; Mitochondria; NAD(P)H Dehydrogenase (Quinone); Optic Atrophies, Hereditary; Quinone Reductases; Rotenone

1989