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Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A. / Calloe, Kirstine; Schmitt, Nicole; Grubb, Søren; Pfeiffer, Ryan; David, Jens-Peter; Kanter, Ronald; Cordeiro, Jonathan M; Antzelevitch, Charles; Callø, Kirstine.
In:
Canadian Journal of Physiology and Pharmacology, Vol. 89, No. 10, 2011, p. 723-36.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Calloe, K
, Schmitt, N, Grubb, S, Pfeiffer, R, David, J-P, Kanter, R, Cordeiro, JM, Antzelevitch, C
& Callø, K 2011, '
Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A',
Canadian Journal of Physiology and Pharmacology, vol. 89, no. 10, pp. 723-36.
https://doi.org/10.1139/y11-070APA
Calloe, K.
, Schmitt, N., Grubb, S., Pfeiffer, R., David, J-P., Kanter, R., Cordeiro, J. M., Antzelevitch, C.
, & Callø, K. (2011).
Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.
Canadian Journal of Physiology and Pharmacology,
89(10), 723-36.
https://doi.org/10.1139/y11-070Vancouver
Calloe K
, Schmitt N, Grubb S, Pfeiffer R, David J-P, Kanter R et al.
Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.
Canadian Journal of Physiology and Pharmacology. 2011;89(10):723-36.
https://doi.org/10.1139/y11-070Author
Calloe, Kirstine ; Schmitt, Nicole ; Grubb, Søren ; Pfeiffer, Ryan ; David, Jens-Peter ; Kanter, Ronald ; Cordeiro, Jonathan M ; Antzelevitch, Charles ; Callø, Kirstine. / Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A. In: Canadian Journal of Physiology and Pharmacology. 2011 ; Vol. 89, No. 10. pp. 723-36.
Bibtex
@article{00c0a620804f4be990b763d6637904a3,
title = "Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A",
abstract = "Mutations in the SCN5A gene have been linked to Brugada syndrome (BrS), conduction disease, Long QT syndrome (LQT3), atrial fibrillation (AF), and to pre- and neonatal ventricular arrhythmias.",
keywords = "Animals, Arrhythmias, Cardiac, CHO Cells, Cell Line, Transformed, Cricetinae, DNA Mutational Analysis, Female, Humans, Infant, Newborn, Ion Channels, Membrane Potentials, Mutation, Missense, NAV1.5 Voltage-Gated Sodium Channel, Patch-Clamp Techniques, Sodium Channels, Syndrome",
author = "Kirstine Calloe and Nicole Schmitt and S{\o}ren Grubb and Ryan Pfeiffer and Jens-Peter David and Ronald Kanter and Cordeiro, {Jonathan M} and Charles Antzelevitch and Kirstine Call{\o}",
year = "2011",
doi = "10.1139/y11-070",
language = "English",
volume = "89",
pages = "723--36",
journal = "Canadian Journal of Physiology and Pharmacology",
issn = "0008-4212",
publisher = "N R C Research Press",
number = "10",
}
RIS
TY - JOUR
T1 - Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A
AU - Calloe, Kirstine
AU - Schmitt, Nicole
AU - Grubb, Søren
AU - Pfeiffer, Ryan
AU - David, Jens-Peter
AU - Kanter, Ronald
AU - Cordeiro, Jonathan M
AU - Antzelevitch, Charles
AU - Callø, Kirstine
PY - 2011
Y1 - 2011
N2 - Mutations in the SCN5A gene have been linked to Brugada syndrome (BrS), conduction disease, Long QT syndrome (LQT3), atrial fibrillation (AF), and to pre- and neonatal ventricular arrhythmias.
AB - Mutations in the SCN5A gene have been linked to Brugada syndrome (BrS), conduction disease, Long QT syndrome (LQT3), atrial fibrillation (AF), and to pre- and neonatal ventricular arrhythmias.
KW - Animals
KW - Arrhythmias, Cardiac
KW - CHO Cells
KW - Cell Line, Transformed
KW - Cricetinae
KW - DNA Mutational Analysis
KW - Female
KW - Humans
KW - Infant, Newborn
KW - Ion Channels
KW - Membrane Potentials
KW - Mutation, Missense
KW - NAV1.5 Voltage-Gated Sodium Channel
KW - Patch-Clamp Techniques
KW - Sodium Channels
KW - Syndrome
U2 - 10.1139/y11-070
DO - 10.1139/y11-070
M3 - Journal article
C2 - 21895525
VL - 89
SP - 723
EP - 736
JO - Canadian Journal of Physiology and Pharmacology
JF - Canadian Journal of Physiology and Pharmacology
SN - 0008-4212
IS - 10
ER -
