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Page 1
Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
PLoS One. 2022 Feb 7;17(2):e0263606. doi: 10.1371/journal.pone.0263606. eCollection 2022.
PLoS One. 2022.
PMID: 35130313
Free PMC article.
Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis.
Alharbi MA, Al-Kafaji G, Khalaf NB, Messaoudi SA, Taha S, Daif A, Bakhiet M.
Alharbi MA, et al. Among authors: daif a.
Biomed Rep. 2019 Dec;11(6):257-268. doi: 10.3892/br.2019.1250. Epub 2019 Nov 4.
Biomed Rep. 2019.
PMID: 31798871
Free PMC article.
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