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Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
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Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
title
Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
main subject
Brugada syndrome
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author
Ryan Pfeiffer
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Kirstine Calloe
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Charles Antzelevitch
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6
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stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Charles Antzelevitch
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
author name string
Jonathan M Cordeiro
series ordinal
1
1 reference
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Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Mark Marieb
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Elena Burashnikov
series ordinal
5
1 reference
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Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
publication date
1 May 2009
1 reference
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Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
published in
Journal of Molecular and Cellular Cardiology
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
volume
46
1 reference
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Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
issue
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
page(s)
695-703
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
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Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias
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Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome
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Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
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Calcium channel inactivation: possible role in signal transduction and Ca2+ signaling
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21 June 2018
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
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21 June 2018
A single CaVbeta can reconstitute both trafficking and macroscopic conductance of voltage-dependent calcium channels
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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations
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21 June 2018
Role of sodium and calcium channel block in unmasking the Brugada syndrome
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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
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Voltage-gated rearrangements associated with differential beta-subunit modulation of the L-type Ca(2+) channel inactivation
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Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome
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Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent
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Brugada syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.YJMCC.2009.01.014
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Unique modulation of L-type Ca2+ channels by short auxiliary beta1d subunit present in cardiac muscle
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Crossref
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retrieved
7 January 2021
Identifiers
DOI
10.1016/J.YJMCC.2009.01.014
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PMC publication ID
2668128
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PubMed publication ID
19358333
1 reference
stated in
Europe PubMed Central
PMC publication ID
2668128
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358333%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
ResearchGate publication ID
24268406
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