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English
Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
scientific article published on 01 December 2000
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
title
Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
author
Teeratorn Pulkes
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Mary G. Sweeney
series ordinal
2
object named as
M G Sweeney
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Michael Hanna
series ordinal
3
object named as
M G Hanna
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
language of work or name
English
0 references
publication date
1 December 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
356
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
9247
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
2068-2069
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
cites work
A tRNA suppressor mutation in human mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2903408-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2903408-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2903408-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2903408-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2903408-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(00)03408-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
11145497
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11145497
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11145497%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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