Human mitochondrial complex I in health and disease (Q24540036)

American Journal of Human Genetics

Europe PubMed Central

title

Human mitochondrial complex I in health and disease (English)

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1 reference

J Smeitink

1

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L van den Heuvel

series ordinal

2

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language of work or name

English

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publication date

June 1999

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published in

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volume

64

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page(s)

1505-10

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issue

6

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cites work

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Tom40 forms the hydrophilic channel of the mitochondrial import pore for preproteins [see comment].

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Deficiency of respiratory chain complex I is a common cause of Leigh disease.

29 November 2018

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Fatal neonatal cardiomyopathy associated with cataract and mitochondrial myopathy

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12 December 2020

Mitochondrial Disorders

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12 December 2020

Yield of mtDNA mutation analysis in 2,000 patients

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12 December 2020

Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art

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12 December 2020

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.

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Crossref

https://api.crossref.org/works/10.1086%2F302432

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302432

1 reference

787445

787445

1 reference

1 reference

1 reference