Isolated complex I deficiency in children: clinical, biochemical and genetic aspects (Q28143420)

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scientific article (publication date: 2000)

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Language	Label	Description	Also known as
English	Isolated complex I deficiency in children: clinical, biochemical and genetic aspects	scientific article (publication date: 2000)

Statements

instance of

scholarly article

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review article

1 reference

stated in

Europe PubMed Central

title

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects (English)

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author name string

J L Loeffen

series ordinal

1

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J A Smeitink

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2

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J M Trijbels

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3

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A J Janssen

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4

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R H Triepels

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5

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R C Sengers

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6

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L P van den Heuvel

series ordinal

7

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language of work or name

English

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publication date

2000

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published in

Human Mutation

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volume

15

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issue

2

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page(s)

123-34

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cites work

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%28200002%2915%3A2%3C123%3A%3AAID-HUMU1%3E3.0.CO%3B2-P

retrieved

21 January 2018

Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%28200002%2915%3A2%3C123%3A%3AAID-HUMU1%3E3.0.CO%3B2-P

retrieved

21 January 2018

Lacticacidemia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%28200002%2915%3A2%3C123%3A%3AAID-HUMU1%3E3.0.CO%3B2-P

retrieved

21 January 2018

The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathology

1 reference

stated in

COCI

retrieved

9 November 2024

reference URL

https://opencitations.net/index/api/v1/citations/10.1023/A:1005402020569

The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients

1 reference

stated in

COCI

retrieved

9 November 2024

reference URL

https://opencitations.net/index/api/v1/citations/10.1023/A:1005434912463

Identifiers

DOI

10.1002/(SICI)1098-1004(200002)15:2<123::AID-HUMU1>3.0.CO;2-P

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10.1002/(SICI)1098-1004(200002)15:2<123::AID-HUMU1>3.3.CO;2-G

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3248478

OpenCitations bibliographic resource ID

3248478

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3248478

PubMed publication ID

10649489

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3248478

 

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