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

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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. / Olsen, N.K.; Hansen, A.W.; Nørby, Søren; Edal, A.L.; Jørgensen, J.R.; Rosenberg, T.

In: Acta Neurologica Scandinavica, No. Vol 91, 1995, p. 326-329.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Olsen, NK, Hansen, AW, Nørby, S, Edal, AL, Jørgensen, JR & Rosenberg, T 1995, 'Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation', Acta Neurologica Scandinavica, no. Vol 91, pp. 326-329.

APA

Olsen, N. K., Hansen, A. W., Nørby, S., Edal, A. L., Jørgensen, J. R., & Rosenberg, T. (1995). Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. Acta Neurologica Scandinavica, (Vol 91), 326-329.

Vancouver

Olsen NK, Hansen AW, Nørby S, Edal AL, Jørgensen JR, Rosenberg T. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. Acta Neurologica Scandinavica. 1995;(Vol 91):326-329.

Author

Olsen, N.K. ; Hansen, A.W. ; Nørby, Søren ; Edal, A.L. ; Jørgensen, J.R. ; Rosenberg, T. / Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. In: Acta Neurologica Scandinavica. 1995 ; No. Vol 91. pp. 326-329.

Bibtex

@article{490da3f074cd11dbbee902004c4f4f50,
title = "Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation",
abstract = "Genetik, Leber's opticusatrofi, dissemineret sclerose, mitokondrie-DNA, mutation",
author = "N.K. Olsen and A.W. Hansen and S{\o}ren N{\o}rby and A.L. Edal and J.R. J{\o}rgensen and T. Rosenberg",
year = "1995",
language = "English",
pages = "326--329",
journal = "Acta Neurologica Scandinavica",
issn = "0001-6314",
publisher = "Wiley-Blackwell",
number = "Vol 91",

}

RIS

TY - JOUR

T1 - Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

AU - Olsen, N.K.

AU - Hansen, A.W.

AU - Nørby, Søren

AU - Edal, A.L.

AU - Jørgensen, J.R.

AU - Rosenberg, T.

PY - 1995

Y1 - 1995

N2 - Genetik, Leber's opticusatrofi, dissemineret sclerose, mitokondrie-DNA, mutation

AB - Genetik, Leber's opticusatrofi, dissemineret sclerose, mitokondrie-DNA, mutation

M3 - Journal article

SP - 326

EP - 329

JO - Acta Neurologica Scandinavica

JF - Acta Neurologica Scandinavica

SN - 0001-6314

IS - Vol 91

ER -

ID: 244701