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

Crossref DOI link: https://doi.org/10.1038/s41598-022-15385-2

Published Online: 2022-06-30

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Al‐Kafaji, Ghada

Alharbi, Maram A.

Alkandari, Hasan

Salem, Abdel Halim

Bakhiet, Moiz
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Text and Data Mining valid from 2022-06-30

Version of Record valid from 2022-06-30
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Article History

Received: 21 February 2022

Accepted: 23 June 2022

First Online: 30 June 2022

Competing interests

: The authors declare no competing interests.

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