Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
about
The genetic basis of Brugada syndrome: a mutation updateA study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease.Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel.Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene.Regulation and physiological function of Nav1.5 and KCNQ1 channels
P2860
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
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2009 nî lūn-bûn
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2009 թուականի Մարտին հրատարակուած գիտական յօդուած
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2009 թվականի մարտին հրատարակված գիտական հոդված
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2009年の論文
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2009年論文
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2009年論文
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2009年論文
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2009年論文
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2009年論文
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2009年论文
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name
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@ast
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
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type
label
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@ast
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@en
prefLabel
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@ast
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@en
P2093
P2860
P50
P1476
Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A
@en
P2093
J Hastrup Svendsen
J Hofman-Bang
M Christiansen
P Cedergreen
P2860
P304
P356
10.1016/S0828-282X(09)70043-1
P577
2009-03-01T00:00:00Z