Therapeutic Options in Hereditary Optic Neuropathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical)
Link
http://link.springer.com/content/pdf/10.1007/s40265-020-01428-3.pdf
Reference247 articles.
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2. Yu-Wai-Man P, Griffiths PG, Chinnery PF. Mitochondrial optic neuropathies—disease mechanisms and therapeutic strategies. Prog Retin Eye Res. 2011;30(2):81–114.
3. La Morgia C, Carbonelli M, Barboni P, Sadun AA, Carelli V. Medical management of hereditary optic neuropathies. Front Neurol. 2014;5:141.
4. Achilli A, Iommarini L, Olivieri A, Pala M, Hooshiar Kashani B, Reynier P, La Morgia C, Valentino ML, Liguori R, Pizza F, Barboni P, et al. Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber’s hereditary optic neuropathy. PLoS ONE. 2012;7(8):e42242.
5. Del Dotto V, Fogazza M, Carelli V, Rugolo M, Zanna C. Eight human opa1 isoforms, long and short: What are they for? Biochim Biophys Acta Bioenergy. 2018;1859(4):263–9.
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