Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q61922622)
Watch
English
Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: a second case
scientific article published in August 2000
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Neuromuscular syndrome associated with the 3291T-->C mutation of mitochondrial DNA: a second case
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author
Tiziana Granata
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Eleonora Lamantea
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Marina Mora
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
G Uziel
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
F Carrara
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
M Zeviani
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 August 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
415-418
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Molecular genetic aspects of human mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation (8342G→A) in the mitochondrial tRNALys gene associated with progressive external ophthalmoplegia and myoclonus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900115-7
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%2FS0960-8966%2899%2900115-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(99)00115-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
10899447
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10899447
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899447%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit