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Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
title
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
main subject
mitochondrial DNA
0 references
heteroplasmy
1 reference
based on heuristic
inferred from title
author
Ian Holt
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
author name string
D H Miller
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
A E Harding
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
language of work or name
English
0 references
publication date
1 December 1989
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
volume
26
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
issue
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
page(s)
739-743
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
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=1015752
retrieved
21 June 2018
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
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=1015752
retrieved
21 June 2018
Maternal inheritance of human mitochondrial DNA
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=1015752
retrieved
21 June 2018
Leber's optic atrophy, a possible example of maternal inheritance.
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=1015752
retrieved
21 June 2018
Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase
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=1015752
retrieved
21 June 2018
Deletions of mitochondrial DNA in Kearns-Sayre syndrome
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=1015752
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=1015752
retrieved
21 June 2018
Mitochondrial DNA-like sequences in the human nuclear genome. Characterization and implications in the evolution of mitochondrial DNA.
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=1015752
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=1015752
retrieved
21 June 2018
Duplications of mitochondrial DNA in mitochondrial myopathy
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=1015752
retrieved
21 June 2018
A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) 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=1015752
retrieved
21 June 2018
Conservation of genes coding for proteins synthesized in human mitochondria
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=1015752
retrieved
21 June 2018
Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2575667
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2575667
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2575667
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2575667
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identical mitochondrial DNA deletion in blood and muscle
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2575667
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.26.12.739
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
PMC publication ID
1015752
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
PubMed publication ID
2575667
1 reference
stated in
Europe PubMed Central
PMC publication ID
1015752
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2575667%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 October 2019
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