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Vilskersts R, Liepinsh E, Kuka J, Cirule H, Veveris M, Kalvinsh I, Dambrova M (2009)
A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population
[DOI] [PMC free article] [PubMed] [Google Scholar] 59.Khalaf D., Krger M., Wehland M., Infanger M., Grimm D
Becker, Sophie Schneitler, Alessandra Morassutti PLOS Neglected Tropical Diseases .2024
Coenzyme Q10 with multiple vitamins is generally ineffective in treatment of mitochondrial disease
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