Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy (Q78059469)

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10 December 2019

title

Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy (English)

1 reference

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hereditary optic neuropathy

10 December 2019

main subject

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3

A H Schapira

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10 December 2019

2

J M Cooper

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10 December 2019

author name string

H R Cock

series ordinal

1

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10 December 2019

publication date

1 May 1999

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Journal of the Neurological Sciences

10 December 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10426140%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

volume

165

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10 December 2019

page(s)

10-17

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10 December 2019

issue

1

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Mitochondrial genetics: a paradigm for aging and degenerative diseases?

10 December 2019

cites work

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Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

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Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy

7 January 2021

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7 January 2021

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In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by31P magnetic resonance spectroscopy

7 January 2021

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The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy

7 January 2021

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(99)00088-X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10426140%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

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