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English
Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C
scientific article published on 27 June 2013
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
title
Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
author
Mark A Tarnopolsky
series ordinal
1
object named as
Mark Tarnopolsky
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
author name string
Brandon Meaney
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Brian Robinson
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Katherine Sheldon
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Richard G Boles
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
publication date
27 June 2013
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
published in
American Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
volume
161A
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
page(s)
2020-2023
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
Identifiers
DOI
10.1002/AJMG.A.36000
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
PubMed ID
23813926
1 reference
stated in
Europe PubMed Central
PubMed ID
23813926
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23813926%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 March 2020
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