Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy (Q33597770)

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scientific article published on November 1, 1991

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Language	Label	Description	Also known as
English	Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy	scientific article published on November 1, 1991

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

main subject

mitochondrial DNA

0 references

hereditary optic neuropathy

1 reference

based on heuristic

inferred from title

genetics

1 reference

stated in

Crossref

DOI

10.1136/JMG.28.11.765

reference URL

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

retrieved

19 November 2022

author

Joanna Poulton

series ordinal

1

object named as

J. Poulton

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

author name string

Bronte-Stewart J

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

M. E. Deadman

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

J. Bronte-Stewart

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

W. S. Foulds

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

R. M. Gardiner

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

language of work or name

English

0 references

publication date

1 November 1991

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

full work available at URL

https://europepmc.org/articles/PMC1017112

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

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

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

reference URL

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

retrieved

19 November 2022

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

1 reference

stated in

Crossref

DOI

10.1136/JMG.28.11.765

reference URL

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

retrieved

19 November 2022

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

volume

28

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

issue

11

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

page(s)

765-770

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

cites work

Sequence and organization of the human mitochondrial genome

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed Central

reference URL

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

retrieved

21 June 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1770533

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1770533

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1770533

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1770533

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1770533

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of single DNA base differences by competitive oligonucleotide priming

series ordinal

14

1 reference

stated in

Crossref

DOI

10.1136/JMG.28.11.765

reference URL

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

retrieved

19 November 2022

Identifiers

DOI

10.1136/JMG.28.11.765

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

PMC publication ID

1017112

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

PubMed publication ID

1770533

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1770533

retrieved

28 July 2017

ResearchGate publication ID

21384324

0 references

 

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