Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia

P J  Laitinen; H  Swan; K  Piippo; M  Viitasalo; L  Toivonen; K  Kontula

doi:10.1080/17431380410032599

Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia

P J Laitinen, H Swan, K Piippo, M Viitasalo, L Toivonen, K Kontula

Forskningsoutput: Tidskriftsbidrag › Översiktsartikel › Peer review

Originalspråk	engelska
Tidskrift	Annals of Medicine
Volym	36
Sidor (från-till)	81-86
Antal sidor	6
ISSN	0785-3890
DOI	https://doi.org/10.1080/17431380410032599
Status	Publicerad - 2004
MoE-publikationstyp	A2 Granska artikel i en vetenskaplig tidskrift

Vetenskapsgrenar

312 Klinisk medicin

Åtkomst av dokument

10.1080/17431380410032599

Citera det här

@article{95f7084230af4e35bdbf3e8aea53569b,

title = "Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia",

keywords = "arrhythmia, catecholaminergic polymorphic ventricular tachycardia, gene mutations, ryanodine receptor, CHANNEL RYANODINE RECEPTOR, CA2+ RELEASE CHANNEL, CALCIUM-RELEASE, CHROMOSOME 1Q42-Q43, MUTATIONS, ARRHYTHMIAS, FKBP12.6, DISEASE, ARVD2, IDENTIFICATION, 312 Clinical medicine",

author = "Laitinen, {P J} and H Swan and K Piippo and M Viitasalo and L Toivonen and K Kontula",

year = "2004",

doi = "10.1080/17431380410032599",

language = "English",

volume = "36",

pages = "81--86",

journal = "Annals of Medicine",

issn = "0785-3890",

publisher = "Taylor & Francis",

}

TY - JOUR

T1 - Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia

AU - Laitinen, P J

AU - Swan, H

AU - Piippo, K

AU - Viitasalo, M

AU - Toivonen, L

AU - Kontula, K

PY - 2004

Y1 - 2004

KW - arrhythmia

KW - catecholaminergic polymorphic ventricular tachycardia

KW - gene mutations

KW - ryanodine receptor

KW - CHANNEL RYANODINE RECEPTOR

KW - CA2+ RELEASE CHANNEL

KW - CALCIUM-RELEASE

KW - CHROMOSOME 1Q42-Q43

KW - MUTATIONS

KW - ARRHYTHMIAS

KW - FKBP12.6

KW - DISEASE

KW - ARVD2

KW - IDENTIFICATION

KW - 312 Clinical medicine

U2 - 10.1080/17431380410032599

DO - 10.1080/17431380410032599

M3 - Review Article

VL - 36

SP - 81

EP - 86

JO - Annals of Medicine

JF - Annals of Medicine

SN - 0785-3890

ER -