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

(2000) JOURNAL OF NEUROLOGY. 247(7). p.535-543
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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.
@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},
}

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