(Q33597770)

28 July 2017

Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy (English)

1 reference

hereditary optic neuropathy

28 July 2017

0 references

1 reference

1 reference

https://api.crossref.org/works/10.1136/JMG.28.11.765

19 November 2022

1

J. Poulton

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

19 November 2022

author name string

Bronte-Stewart J

3

1 reference

28 July 2017

M. E. Deadman

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

19 November 2022

J. Bronte-Stewart

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

19 November 2022

W. S. Foulds

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

19 November 2022

R. M. Gardiner

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

19 November 2022

language of work or name

English

0 references

publication date

1 November 1991

1 reference

full work available at URL

28 July 2017

https://europepmc.org/articles/PMC1017112

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

https://europepmc.org/articles/PMC1017112?pdf=render

19 November 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1770533

https://syndication.highwire.org/content/doi/10.1136/jmg.28.11.765

19 November 2022

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1136/JMG.28.11.765

Journal of Medical Genetics

19 November 2022

published in

1 reference

28 July 2017

28

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28 July 2017

765-770

1 reference

28 July 2017

11

1 reference

Sequence and organization of the human mitochondrial genome

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017112

Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy

21 June 2018

1 reference

12 December 2020

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

12 December 2020

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy

1 reference

12 December 2020

The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease

1 reference

12 December 2020

The inheritance of Leber's disease. A genealogical follow-up study

1 reference

12 December 2020

Detection of single DNA base differences by competitive oligonucleotide priming

14

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1136/JMG.28.11.765

19 November 2022

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

1 reference