Mitochondrial Optic Neuropathies: How Two Genomes may Kill the Same Cell Type?
Author:
Affiliation:
1. Laboratory of Neurogenetics, Department of Neurological Sciences, University of Bologna, Via Ugo Foscolo 7, Bologna 40123, Italy
Abstract
Publisher
Portland Press Ltd.
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Link
https://portlandpress.com/bioscirep/article-pdf/27/1-3/173/474469/bsr0270173.pdf
Reference73 articles.
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2. Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM Elsas LJ, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy. Science 242:1427–1430
3. Von Graefe A (1858) Ein ungewőhnlicher Fall von hereditarer Amaurose. Arch Ophthalmol 4:266–268
4. Leber T (1871) Uber hereditare und congenital-angelegte Sehnervenleiden. Arch Ophthalmol 17:249–291
5. Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM (2000) The epidemiology of pathogenic mitochondrial DNA mutations. Ann Neurol 48:188–193
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