(Q35243833)

7 August 2017

1 reference

title

Disorders associated with multiple deletions of mitochondrial DNA (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

author name string

M. Haltia

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

A. Suomalainen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

A. Majander

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

H. Somer

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1341954

16 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1341954

16 September 2022

publication date

1 April 1992

1 reference

7 August 2017

1 reference

7 August 2017

volume

2

1 reference

7 August 2017

issue

2

1 reference

7 August 2017

page(s)

133-139

1 reference

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

7 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Deletion of blood mitochondrial DNA in pancytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Directly repeated sequences associated with pathogenic mitochondrial DNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Characterization of a mitochondrial protein binding to single-stranded DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Detection of a specific mitochondrial DNA deletion in tissues of older humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Mitochondrial DNA mutations and neuromuscular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1992.TB00681.X

10.1111/J.1750-3639.1992.TB00681.X

21 January 2018

Identifiers

DOI

1 reference

7 August 2017

1 reference