(Q34420013)

2 August 2017

1 reference

title

Mutations in mitochondrial DNA as a cause of exercise intolerance (English)

1 reference

2 August 2017

0 references

DiMauro S

1

1 reference

PubMed ID

11680795

2 August 2017

Andreu AL

series ordinal

2

1 reference

PubMed ID

11680795

2 August 2017

language of work or name

English

0 references

publication date

1 October 2001

1 reference

2 August 2017

1 reference

2 August 2017

33

1 reference

2 August 2017

7

1 reference

2 August 2017

472-476

1 reference

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

2 August 2017

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

Exercise intolerance resulting: from a muscle-restricted mutation in the mitochondrial tRNALeu(CUN)gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F07853890109002096

10.3109/07853890109002096

21 January 2018

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11680795