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Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

✍ Scribed by N. K. Olsen; A. W. Hansen; S. Nørby; A. L. Edal; J. R. Jørgensen; T. Rosenberg

Book ID: 114784531
Publisher: John Wiley and Sons
Year: 1995
Tongue: English
Weight: 511 KB
Volume: 91
Category: Article
ISSN: 0001-6314
DOI: 10.1111/j.1600-0404.1995.tb07016.x

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