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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2024. (Total: 234082Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Sclerosis and ND2[original query]
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
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
Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis.
Biomedical reports 2019 12 11 (6): 257-268.
Alharbi Maram Atallah, Al-Kafaji Ghada, Khalaf Noureddine Ben, Messaoudi Safia Abdulsalam, Taha Safa, Daif Abdulqader, Bakhiet Mo
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
PloS one 2022 17 (2): e0263606.
Al-Kafaji Ghada, Bakheit Halla F, AlAli Faisal, Fattah Mina, Alhajeri Saad, Alharbi Maram A, Daif Abdulqader, Alsabbagh Manahel Mahmood, Alwehaidah Materah Salem, Bakhiet Mo
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