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LMNA mutations in atypical Werner's syndrome
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instance of
scholarly article
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title
LMNA mutations in atypical Werner's syndrome
(English)
0 references
author
Gisèle Bonne
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
Nicolas Levy
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
author name string
Gisele Bonne
series ordinal
1
0 references
Nicolas Levy
series ordinal
2
0 references
language of work or name
English
0 references
publication date
November 2003
0 references
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
volume
362
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
issue
9395
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
page(s)
1585-6; author reply 1586
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
cites work
LMNA mutations in atypical Werner's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914761-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914761-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914761-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical relevance of atrial fibrillation/flutter, stroke, pacemaker implant, and heart failure in Emery-Dreifuss muscular dystrophy: a long-term longitudinal study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914761-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(03)14761-7
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
PubMed ID
14615129
1 reference
stated in
Europe PubMed Central
PubMed ID
14615129
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14615129%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 May 2020
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