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Query Trace: Multiple Sclerosis and ND1[orginal query]

Mitochondrial DNA T4216C and A4917G variations in multiple sclerosis. Journal of the neurological sciences 2015 Sep 356 (1-2): 55-60. Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Gjedde Albe Similar articles in PubMed
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 Similar articles in PubMed
Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients. Cellular and molecular neurobiology 2007 Sep 27 (6): 695-700. Ahari Solmaz Etemad, Houshmand Massoud, Panahi Mehdi Shafa Shariat, Kasraie Sadaf, Moin Mostafa, Bahar Mohammad A Similar articles in PubMed
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 Similar articles in PubMed