About: Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois

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About: Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в грудні 2005 (uk) artículu científicu espublizáu n'avientu de 2005 (ast) scientific article published on 01 December 2005 (en)
publication date	wds:Q81606752-67F6C60A-731A-4C0C-A7EB-FD9D04A44B1B
publication date	2005-12-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q81606752-4F1E570A-C8D3-4931-A94C-DA2DB873C955
author name string	Jeffrey E Saffitz
rdfs:label	Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (en) Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (nl)
skos:prefLabel	Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (en) Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (nl)
name	Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (en) Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (nl)
title	wds:Q81606752-6849DA14-2509-4573-9D07-1DD131A0CA0D
title	Structural heart disease, SCN5A gene mutations, and Brugada syndrome: a complex ménage à trois (en)
page(s)	wds:Q81606752-C140308F-66BE-4810-BC86-5E15B486B133
page(s)	3672-3674
instance of	wds:Q81606752-A07A7A04-6938-491F-BF2C-04D60C801095
instance of	scholarly article
main subject	wds:Q81606752-3D699119-86BE-4EAF-A6CE-70169BCBC626
main subject	Brugada syndrome
PubMed ID	wds:Q81606752-8EA23AAC-31F4-45B5-898E-6CA313F74E07
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16344397
PubMed ID	16344397
published in	wds:Q81606752-77DE887B-06EF-4283-BAD8-D60C37A1BBEA
published in	Circulation
issue	wds:Q81606752-66A158F6-F90E-487B-9E5A-727E321B3FE1
volume	wds:Q81606752-BDA9C202-9877-4245-9757-CD4596878AD7
issue	24
volume	112
DOI	wds:Q81606752-71D7B75B-42B7-4413-8630-59443795C51E
DOI	http://dx.doi.org/10.1161/CIRCULATIONAHA.105.587147
DOI	10.1161/CIRCULATIONAHA.105.587147
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81606752
is cites work of	Brugada syndrome The genetic basis of long QT and short QT syndromes: a mutation update The genetic basis of Brugada syndrome: a mutation update Network-based approach to prediction and population-based validation of in silico drug repurposing. Mutations in voltage-gated L-type calcium channel: implications in cardiac arrhythmia
is cites work of	wds:Q61608949-4C409E09-0A6C-43B0-B09D-23C407C7D6E2 wds:Q28262724-07F568CA-1CB6-4383-862B-4A605CA6C178 wds:Q55643995-974F877A-5E3B-40DF-921F-8D36E5C6CC53 wds:Q28252115-972B5D81-52AD-442C-BD2D-338DD4E13A18 wds:Q58777181-A3FE955E-C703-49D5-BA9E-AE41A2B85361

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