Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis.
Journal of the neurological sciences 2014 Oct 345 (1-2): 220-3.
Poursadegh Zonouzi Ahmad, Ghorbian Saeid, Abkar Morteza, Poursadegh Zonouzi Ali Akbar, Azadi A
Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.
European neurology 2004 51 (2): 68-71.
Houshmand M, Sanati M-H, Rashedi I, Sharifpanah F, Asghari E, Lotfi