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Leigh syndrome

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

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

published 07 Feb 2022

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Degree of Glutathione Deficiency and Redox Imbalance Depend on Subtype of Mitochondrial Disease and Clinical Status

Gregory M. Enns, Tereza Moore, Anthony Le, Kondala Atkuri, Monisha K. Shah, Kristina Cusmano-Ozog, Anna-Kaisa Niemi, Tina M. Cowan

published 18 Jun 2014

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