Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis

por Al-Kafaji, Ghada, Alwehaidah, Materah Salem, Alsabbagh, Manahel Mahmood, Alharbi, Maram A., Bakhiet, Moiz
Publicado 2022

Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis

por Al-Kafaji, Ghada, Bakheit, Halla F., AlAli, Faisal, Fattah, Mina, Alhajeri, Saad, Alharbi, Maram A., Daif, Abdulqader, Alsabbagh, Manahel Mahmood, Alwehaidah, Materah Salem, Bakhiet, Moiz
Publicado 2022