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

Authors

Anne Chiaramello, George Washington University

Document Type

Journal Article

Publication Date

6-18-2018

Journal

Mitochondrion

APA Citation

Chiaramello, A. (2018). The m.11778A>G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metaboloc interplay between mitochondrial oxidative phosphorylation and glycolysis. Mitochondrion, (). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_anatregbio_facpubs/542