Mutational analysis of RyR2 gene in patients after arrhythmic storm

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F12%3A%230001621" target="_blank" >RIV/65269705:_____/12:#0001621 - isvavai.cz</a>

Result on the web

<a href="http://dx.doi.org/10.1016/j.crvasa.2012.03.003" target="_blank" >http://dx.doi.org/10.1016/j.crvasa.2012.03.003</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.crvasa.2012.03.003" target="_blank" >10.1016/j.crvasa.2012.03.003</a>

Result language

angličtina

Original language name

Mutational analysis of RyR2 gene in patients after arrhythmic storm

Original language description

Mutations of RyR2 gene encoding calcium channel of sarcoplazmatic reticulum are the cause of congenital catecholaminergic polymorphic ventricular tachycardia. The aim of this study was to test the hypothesis that RyR2 variants can increase occurrence ofmalignant arrhythmias in patients with structural heart diseases.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FD - Oncology and haematology

OECD FORD branch

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Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2012

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Cor et Vasa

ISSN

0010-8650

e-ISSN

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Volume of the periodical

54

Issue of the periodical within the volume

3-4

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

4

Pages from-to

127-130

UT code for WoS article

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EID of the result in the Scopus database

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