Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
about
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature.
P2860
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@ast
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@en
type
label
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@ast
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@en
prefLabel
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@ast
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@en
P2093
P2860
P1476
Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation.
@en
P2093
Daniel Kroening
David Huang
Gabriel Vorobiof
Ramon Brugada
P2860
P304
P356
10.1111/J.1540-8159.2008.01056.X
P577
2008-05-01T00:00:00Z