Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited cardiac disorder caused by mutations predominantly in the ryanodine receptor (RyR2) gene. We sought to identify mutations in genes affecting cardiac calcium cycling in patients with CPVT and in less typica...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Marjamaa, Annukka, Laitinen-Forsblom, Päivi, Lahtinen, Annukka M, Viitasalo, Matti, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2009
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2667497/
https://ncbi.nlm.nih.gov/pubmed/19216760
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-12
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