Recurrent optic neuropathy: a case of Harding’s disease?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06542-6.pdf
Reference7 articles.
1. Wallace DC, et al. (1988) Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy. Science (80-. ) 242(4884): 1427–1430. https://doi.org/10.1126/science.3201231
2. Pfeffer G, Burke A, Yu-Wai-Man P, Compston DAS, Chinnery PF (2013) Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations. Neurology 81(24):2073–2081. https://doi.org/10.1212/01.wnl.0000437308.22603.43
3. Brown MD, Sun F, Wallace DC (1997) Clustering of Caucasian leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet 60(2):381–387
4. Palace J (2009) Multiple sclerosis associated with Leber’s hereditary optic neuropathy. J Neurol Sci 286(1–2):24–27. https://doi.org/10.1016/j.jns.2009.09.009
5. Balasopoulou A et al (2017) Symposium recent advances and challenges in the management of retinoblastoma globe - saving treatments. BMC Ophthalmol 17(1):1. https://doi.org/10.4103/ijo.IJO
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