(Q47852503)

English

Nuclear power and mitochondrial disease

scientific article published in July 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

Nuclear power and mitochondrial disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

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author name string

DiMauro S

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

Schon EA

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

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publication date

1 July 1998

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

Nature Genetics

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

19

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

3

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

214-215

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

Molecular genetic aspects of human mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1038%2F883

7 January 2021

based on heuristic

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The development of mitochondrial medicine

1 reference

https://api.crossref.org/works/10.1038%2F883

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA mutations and pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2F883

7 January 2021

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Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

1 reference

https://api.crossref.org/works/10.1038%2F883

7 January 2021

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Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

1 reference

https://api.crossref.org/works/10.1038%2F883

7 January 2021

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Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

1 reference

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Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

1 reference

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Localization of the Wilson's disease protein product to mitochondria

1 reference

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Oxidative stress and mitochondrial dysfunction in neurodegeneration

1 reference

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

1 reference

https://api.crossref.org/works/10.1038%2F883

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Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit

1 reference

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7 January 2021

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Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

release_xtjeh2k37bdvpc5djaeyaejmwy

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https://api.fatcat.wiki/v0/release/xtjeh2k37bdvpc5djaeyaejmwy

24 November 2022

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mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9662387

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