LHON mutations in Italian patients affected by multiple sclerosis
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1997.tb00257.x/fullpdf
Reference26 articles.
1. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation;Harding;Brain,1992
2. Parent-child concordance in multiple sclerosis;Sadovnick;Ann Neurol,1991
3. Spectrum of mitochondrial DNA mutations in Leber's hereditary optic neuropathy;Brown;Clin Neurosci,1994
4. Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation;Oostra;Hum Genet,1994
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2. Lack of association between mitochondrial DNA G15257A and G15812A variations and multiple sclerosis;Journal of the Neurological Sciences;2015-09
3. Differential diagnosis of Mendelian and mitochondrial disorders in patients with suspected multiple sclerosis;Brain;2015-01-29
4. Multiple sclerosis and mitochondrial gene variations: A review;Journal of the Neurological Sciences;2013-07
5. Multiple sclerosis associated with Leber's Hereditary Optic Neuropathy;Journal of the Neurological Sciences;2009-11
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