Analysis of the entire mitochondrial genome reveals Leber’s hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis

por Al‐Kafaji, Ghada, Alharbi, Maram A., Alkandari, Hasan, Salem, Abdel Halim, Bakhiet, Moiz
Publicado 2022

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