Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation

Mikael Koponen; Annukka Marjamaa; Annukka M. Tuiskula; Matti Viitasalo; Terhi Nallinmaa-Luoto; Jaakko T. Leinonen; Elisabeth Widen; Lauri Toivonen; Kimmo Kontula; Heikki Swan

doi:10.1371/journal.pone.0243649

Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation

Mikael Koponen, Annukka Marjamaa, Annukka M. Tuiskula, Matti Viitasalo, Terhi Nallinmaa-Luoto, Jaakko T. Leinonen, Elisabeth Widen, Lauri Toivonen, Kimmo Kontula, Heikki Swan

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Article number	0243649
Journal	PLoS One
Volume	15
Issue number	12
Number of pages	12
ISSN	1932-6203
DOIs	https://doi.org/10.1371/journal.pone.0243649
Publication status	Published - 14 Dec 2020
MoE publication type	A1 Journal article-refereed

Fields of Science

SUDDEN CARDIAC DEATH
MOLECULAR CHARACTERIZATION
BETA-BLOCKERS
ARRHYTHMIAS
GENE
ASSOCIATION
FLECAINIDE
CHILDREN
THERAPY
EVENTS
3121 General medicine, internal medicine and other clinical medicine

Access to Document

10.1371/journal.pone.0243649

pone.0243649Final published version, 608 KBLicence: CC BY

Cite this

Koponen, M., Marjamaa, A., Tuiskula, A. M., Viitasalo, M., Nallinmaa-Luoto, T., Leinonen, J. T., Widen, E., Toivonen, L., Kontula, K., & Swan, H. (2020). Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. PLoS One, 15(12), [0243649]. https://doi.org/10.1371/journal.pone.0243649

@article{cd6884d8d62348dab3b29700c940996e,

title = "Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation",

keywords = "SUDDEN CARDIAC DEATH, MOLECULAR CHARACTERIZATION, BETA-BLOCKERS, ARRHYTHMIAS, GENE, ASSOCIATION, FLECAINIDE, CHILDREN, THERAPY, EVENTS, 3121 General medicine, internal medicine and other clinical medicine",

author = "Mikael Koponen and Annukka Marjamaa and Tuiskula, {Annukka M.} and Matti Viitasalo and Terhi Nallinmaa-Luoto and Leinonen, {Jaakko T.} and Elisabeth Widen and Lauri Toivonen and Kimmo Kontula and Heikki Swan",

year = "2020",

month = dec,

day = "14",

doi = "10.1371/journal.pone.0243649",

language = "English",

volume = "15",

journal = "PLoS One",

issn = "1932-6203",

publisher = "PUBLIC LIBRARY OF SCIENCE",

number = "12",

}

TY - JOUR

T1 - Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation

AU - Koponen, Mikael

AU - Marjamaa, Annukka

AU - Tuiskula, Annukka M.

AU - Viitasalo, Matti

AU - Nallinmaa-Luoto, Terhi

AU - Leinonen, Jaakko T.

AU - Widen, Elisabeth

AU - Toivonen, Lauri

AU - Kontula, Kimmo

AU - Swan, Heikki

PY - 2020/12/14

Y1 - 2020/12/14

KW - SUDDEN CARDIAC DEATH

KW - MOLECULAR CHARACTERIZATION

KW - BETA-BLOCKERS

KW - ARRHYTHMIAS

KW - GENE

KW - ASSOCIATION

KW - FLECAINIDE

KW - CHILDREN

KW - THERAPY

KW - EVENTS

KW - 3121 General medicine, internal medicine and other clinical medicine

U2 - 10.1371/journal.pone.0243649

DO - 10.1371/journal.pone.0243649

M3 - Article

VL - 15

JO - PLoS One

JF - PLoS One

SN - 1932-6203

IS - 12

M1 - 0243649

ER -