(Q34705316)

4 August 2017

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title

Succinate dehydrogenase and human diseases: new insights into a well-known enzyme (English)

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4 August 2017

2

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Agnès Rötig

series ordinal

3

object named as

Agnès Rötig

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4 August 2017

Pierre Rustin

1

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4 August 2017

publication date

1 May 2002

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European Journal of Human Genetics

4 August 2017

published in

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4 August 2017

volume

10

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4 August 2017

issue

5

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4 August 2017

page(s)

289-291

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Inborn errors of complex II--unusual human mitochondrial diseases

4 August 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Phenotypic dichotomy in mitochondrial complex II genetic disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Modulation of mitochondrial succinate dehydrogenase activity, mechanism and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Succinate-driven reverse electron transport in the respiratory chain of plant mitochondria. The effects of rotenone and adenylates in relation to malate and oxaloacetate metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Fluxes of nicotinamide adenine dinucleotides through mitochondrial membranes in human cultured cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Biochemical, physiological and medical aspects of ubiquinone function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Mitochondria, oxygen free radicals, disease and ageing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Clinical spectrum and diagnosis of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

7 January 2021

Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

7 January 2021

The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

7 January 2021

Redox control of beta-oxidation in rat liver mitochondria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

7 January 2021

Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200793

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200793

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Dimensions Publication ID

4 August 2017

1019189868

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