How defective mitochondrial electrical activity leads to inherited blindness-Reference-Cited by-同舟云学术

How defective mitochondrial electrical activity leads to inherited blindness

Published:2023-10-25 Issue:45 Volume:120 Page:
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proc. Natl. Acad. Sci. U.S.A.

Author:

Burke Peter J.¹²³⁴

Affiliation:

1. Department of Electrical Engineering and Computer Science, University of California, Irvine, CA 92697

2. Department of Biomedical Engineering, University of California, Irvine, CA 92697

3. Department of Chemical and Biomolecular Engineering, University of California, Irvine, CA 92697

4. Department of Materials Science and Engineering, University of California, Irvine, CA 92697

Funder

National Science Foundation

DOD | USA | AFC | CCDC | Army Research Office

HHS | NIH | National Cancer Institute

DOD | USAF | AMC | Air Force Office of Scientific Research

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Link

https://pnas.org/doi/pdf/10.1073/pnas.2315649120

Reference21 articles.

1. Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

2. D. C. Wallace, M. T. Lott, V. Procaccio, “Mitochondrial biology and medicine” in Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics: Foundations, (Elsevier, 2018), pp. 267–322.

3. Mitochondrial dysfunction as a cause of optic neuropathies

4. Coenzyme Q10 trapping in mitochondrial complex I underlies Leber’s hereditary optic neuropathy

5. Key role of quinone in the mechanism of respiratory complex I

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