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English
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
scientific article published on 01 September 1996
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
main subject
long QT syndrome
1 reference
based on heuristic
inferred from title
author
Francis Collins
series ordinal
3
object named as
F S Collins
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
author name string
M W Russell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
M Dick
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
L C Brody
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
publication date
1 September 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Human Molecular Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
1319-1324
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
9
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Identifiers
DOI
10.1093/HMG/5.9.1319
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed ID
8872472
1 reference
stated in
Europe PubMed Central
PubMed ID
8872472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8872472%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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