Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy
Author:
Funder
U.S. Department of Health & Human Services | NIH | National Eye Institute
Canada Research Chairs
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-43180-z.pdf
Reference23 articles.
1. Dimitriadis, K. et al. Leber’s hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients. Orphanet J. Rare Dis. 9, 158, https://doi.org/10.1186/s13023-014-0158-9 (2014).
2. Spruijt, L. et al. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy. Am. J. Ophthalmol. 141, 676–682, https://doi.org/10.1016/j.ajo.2005.11.007 (2006).
3. Puomila, A. et al. Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland. Eur. J. Hum. Genet. 15, 1079–1089, https://doi.org/10.1038/sj.ejhg.5201828 (2007).
4. Gorman, G. S. et al. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Ann. Neurol. 77, 753–759, https://doi.org/10.1002/ana.24362 (2015).
5. Barboni, P. et al. Leber’s hereditary optic neuropathy with childhood onset. Invest. Ophthalmol. Vis. Sci. 47, 5303–5309, https://doi.org/10.1167/iovs.06-0520 (2006).
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