Title

The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis.

Document Type

Journal Article

Publication Date

5-1-2019

Journal

Mitochondrion

Volume

46

Inclusive Pages

187-194

DOI

10.1016/j.mito.2018.06.001

Keywords

Adult; DNA, Mitochondrial; Female; Fibroblasts; Glycolysis; Humans; Mitochondria; Multiple Sclerosis; Optic Atrophy, Hereditary, Leber; Oxidative Phosphorylation; Point Mutation

Comments

Epub 2018 Jun 8

Peer Reviewed

1

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