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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
N. K. Olsen, A. W. Hansen, S. Nørby, A. L. Edal, J. R. Jørgensen, T. RosenbergVolume:
91
Year:
1995
Language:
english
Pages:
4
DOI:
10.1111/j.1600-0404.1995.tb07016.x
File:
PDF, 511 KB
english, 1995