Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73826034)
Watch
English
Drawing the line in progeria syndromes
scientific article published on 01 August 2003
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Drawing the line in progeria syndromes
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
main subject
progeria
1 reference
based on heuristic
inferred from title
author name string
Robert A Hegele
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
language of work or name
English
0 references
publication date
1 August 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
362
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
9382
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
416-417
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
Mechanisms of ageing: public or private?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of the Werner's syndrome gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lamin a truncation in Hutchinson-Gilford progeria.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
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%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premature atherosclerosis associated with monogenic insulin resistance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Life at the edge: the nuclear envelope and human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The nuclear lamina and inherited disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914097-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(03)14097-4
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed ID
12927424
1 reference
stated in
Europe PubMed Central
PubMed ID
12927424
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12927424%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Â
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