(Q71872895)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609444%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609444%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

21 October 2019

main subject

1 reference

5

1 reference

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21 October 2019

author name string

J C Cornelissen

1

1 reference

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21 October 2019

R J Wanders

2

1 reference

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21 October 2019

P A Bolhuis

3

1 reference

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21 October 2019

E Bleeker-Wagemakers

4

1 reference

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21 October 2019

F A Wijburg

6

1 reference

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21 October 2019

publication date

1 January 1993

1 reference

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Journal of Inherited Metabolic Disease

21 October 2019

published in

1 reference

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21 October 2019

volume

16

1 reference

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21 October 2019

issue

3

1 reference

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21 October 2019

page(s)

531-533

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00711673

21 October 2019

exact match

0 references

cites work

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

1 reference

12 December 2020

Leber's hereditary optic neuropathy and complex I deficiency in muscle.

1 reference

12 December 2020

Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblasts

1 reference

12 December 2020

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases

1 reference

12 December 2020

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

1 reference

12 December 2020

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711673

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609444%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference