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Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

L VANOPDENBOSCH, B DUBOIS, MB D'HOOGHE, Françoise Meire UGent and H CARTON (2000) JOURNAL OF NEUROLOGY. 247(7). p.535-543
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
JOURNAL OF NEUROLOGY
J. Neurol.
volume
247
issue
7
pages
535-543 pages
Web of Science type
Article
Web of Science id
000088601600009
ISSN
0340-5354
language
English
UGent publication?
yes
classification
A1
id
172235
handle
http://hdl.handle.net/1854/LU-172235
date created
2004-01-14 13:40:00
date last changed
2016-12-19 15:38:43
@article{172235,
  author       = {VANOPDENBOSCH, L and DUBOIS, B and D'HOOGHE, MB and Meire, Fran\c{c}oise and CARTON, H},
  issn         = {0340-5354},
  journal      = {JOURNAL OF NEUROLOGY},
  language     = {eng},
  number       = {7},
  pages        = {535--543},
  title        = {Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.},
  volume       = {247},
  year         = {2000},
}

Chicago
VANOPDENBOSCH, L, B DUBOIS, MB D’HOOGHE, Françoise Meire, and H CARTON. 2000. “Mitochondrial Mutations of Leber’s Hereditary Optic Neuropathy: a Risk Factor for Multiple Sclerosis.” Journal of Neurology 247 (7): 535–543.
APA
VANOPDENBOSCH, L., DUBOIS, B., D’HOOGHE, M., Meire, F., & CARTON, H. (2000). Mitochondrial mutations of Leber’s hereditary optic neuropathy: a risk factor for multiple sclerosis. JOURNAL OF NEUROLOGY, 247(7), 535–543.
Vancouver
1.
VANOPDENBOSCH L, DUBOIS B, D’HOOGHE M, Meire F, CARTON H. Mitochondrial mutations of Leber’s hereditary optic neuropathy: a risk factor for multiple sclerosis. JOURNAL OF NEUROLOGY. 2000;247(7):535–43.
MLA
VANOPDENBOSCH, L, B DUBOIS, MB D’HOOGHE, et al. “Mitochondrial Mutations of Leber’s Hereditary Optic Neuropathy: a Risk Factor for Multiple Sclerosis.” JOURNAL OF NEUROLOGY 247.7 (2000): 535–543. Print.