Leber hereditary optic neuropathy: a nuclear solution of a mitochondrial problem

Larsson, N.G.

doi:10.1002/ana.10387

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Leber hereditary optic neuropathy: a nuclear solution of a mitochondrial problem

Larsson, N. (2002). Leber hereditary optic neuropathy: a nuclear solution of a mitochondrial problem. Ann Neurol, 52(5), 529-30. doi:10.1002/ana.10387.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000B-71D2-8 Version Permalink: https://hdl.handle.net/21.11116/0000-000B-71D3-7

Genre: Journal Article

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Larsson, N.G.¹, Author

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1Department Larsson - Mitochondrial Biology, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_1942286

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Free keywords: DNA, Mitochondrial/physiology Genetic Therapy Humans Mutation/physiology Optic Atrophy, Hereditary, Leber/*genetics/metabolism/therapy Oxidative Phosphorylation

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Dates: Published Online: 2002-11Date issued: 2002-10-29

Publication Status: Issued

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Identifiers: Other: 12402246
DOI: 10.1002/ana.10387
ISSN: 0364-5134 (Print)0364-5134

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Title: Ann Neurol

Alternative Title : Annals of neurology

Source Genre: Journal

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Pages: - Volume / Issue: 52 (5) Sequence Number: - Start / End Page: 529 - 30 Identifier: -