Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

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 journalJournal articleResearchpeer-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/y11-070

APA

Calloe, K., Schmitt, N., Grubb, S., Pfeiffer, R., David, J-P., Kanter, R., ... 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/y11-070

Vancouver

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/y11-070

Author

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 -

ID: 33964949