(Q35196357)

7 August 2017

Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy (English)

1 reference

7 August 2017

6

Munnich A

1 reference

7 August 2017

Cormier V

1

1 reference

7 August 2017

Rotig A

2

1 reference

7 August 2017

Tardieu M

3

1 reference

7 August 2017

Colonna M

4

1 reference

7 August 2017

Saudubray JM

5

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 April 1991

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

48

1 reference

7 August 2017

643-648

1 reference

7 August 2017

4

1 reference

An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Shuttling of integrated vectors from mammalian cells to E. coli is mediated by head-to-tail multimeric inserts.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Deletion of blood mitochondrial DNA in pancytopenia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682949

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

8 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2014791

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2014791

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1682949

1 reference

7 August 2017

1 reference