Progress in diagnosis and treatment of Leber’s hereditary optic neuropathy
Author:
Funder
National Natural Science Foundation of China
National Natural Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Drug Discovery,Molecular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00109-023-02389-2.pdf
Reference47 articles.
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2. Kellar-Wood H et al (1994) Leber’s hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Ann Neurol 36(1):109
3. Balsa E et al (2012) NDUFA4 is a subunit of complex IV of the mammalian electron transport chain. Cell Metab 16(3):378–386
4. Zickermann V, Wirth C, Nasiri H, Siegmund K, Schwalbe H, Hunte C, Brandt U (2015) Mechanistic insight from the crystal structure of mitochondrial complex I. Science 347(6217):44–49
5. Moser CC et al (2006) Electron tunneling chains of mitochondria. Biochim Biophys Acta Bioenerg (BBA) 1757(9–10):1096–1109
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