No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(92)81482-2/fullpdf
Reference9 articles.
1. Mitochondria and Leber's Hereditary Optic Neuropathy
2. Report of the committee on human mitochondrial DNA
3. Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy
4. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
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1. Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathies;Ophthalmic Genetics;2010-11-11
2. LHON mutations in Italian patients affected by multiple sclerosis;Acta Neurologica Scandinavica;2009-01-29
3. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003
4. Leber hereditary optic neuropathy: clinical and molecular genetic findings;Neurogenetics;2001-05-16
5. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999
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