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

Several mitochondrial DNA (mtDNA) mutations of Leber's hereditary optic neuropathy (LHON) have been reported in patients with multiple sclerosis (MS) from different ethnicities. To further study the involvement of LHON mtDNA mutations in MS in the Arab population, we analyzed sequencing data of...

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Detalles Bibliográficos
Autores principales: Al‐Kafaji, Ghada, Alharbi, Maram A., Alkandari, Hasan, Salem, Abdel Halim, Bakhiet, Moiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246974/
https://www.ncbi.nlm.nih.gov/pubmed/35773337
http://dx.doi.org/10.1038/s41598-022-15385-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246974/
https://www.ncbi.nlm.nih.gov/pubmed/35773337
http://dx.doi.org/10.1038/s41598-022-15385-2

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