Associated Papers
Analysis of the entire mitochondrial genome reveals Leber's hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis.
Al-Kafaji G et al.
Scientific Reports, 2022
Human clinical mutations in mitochondrially encoded subunits of Complex I can be successfully modeled in E. coli.
Zhang F et al.
Mitochondrion, 2022
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
Al-Kafaji G et al.
Plos One, 2022
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