(Q39989238)

English

Complements of the house

scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Complements of the house (English)

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Europe PubMed Central

PMC publication ID

16 September 2017

author name string

Eric A Schon

1

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

language of work or name

0 references

publication date

1 September 2004

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

114

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

6

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

760-762

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

Genetic defects in the oxidative phosphorylation (OXPHOS) system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

Mitochondrial respiratory-chain diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516272

22 September 2017

Identifiers

10.1172/JCI22942

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 September 2017

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