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Mitochondrial 3243 A-->G mutation (MELAS mutation) associated with painful muscle stiffness
scientific article published on 01 July 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
title
Mitochondrial 3243 A-->G mutation (MELAS mutation) associated with painful muscle stiffness
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
main subject
muscle stiffness
1 reference
based on heuristic
inferred from title
author name string
M Deschauer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
T Wieser
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
S Neudecker
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
A Lindner
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
S Zierz
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
publication date
1 July 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
page(s)
305-307
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
cites work
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical features of melas and mitochondrial DNA mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) mtDNA mutation that induces subacute dementia which mimicks Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS point mutation with unusual clinical presentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Did de novo MELAS common mitochondrial DNA point mutation (mtDNA 3243, A-->G transition) occur in the mother of a proband of a Japanese MELAS pedigree?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Melas: an original case and clinical criteria for diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS: clinical features, biochemistry, and molecular genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical features of mitochondrial myopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900019-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(99)00019-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
PubMed publication ID
10407850
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10407850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10407850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
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