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English
Mutations in the Complex III Assembly Factor Tetratricopeptide 19 Gene TTC19 Are a Rare Cause of Leigh Syndrome
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
case report
0 references
title
Mutations in the Complex III Assembly Factor Tetratricopeptide 19 Gene TTC19 Are a Rare Cause of Leigh Syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
author
Paldeep S Atwal
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
author name string
P S Atwal
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
24368687
retrieved
2 August 2017
publication date
25 December 2013
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
published in
Journal of Inherited Metabolic Disorders Reports
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
volume
14
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
page(s)
43-45
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
cites work
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies
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=4213333
retrieved
6 July 2018
Identifiers
DOI
10.1007/8904_2013_282
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
PMC publication ID
4213333
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
PubMed publication ID
24368687
1 reference
stated in
Europe PubMed Central
PMC publication ID
4213333
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24368687%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
ResearchGate publication ID
259462682
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