Linked Life Data

17081365

Source:http://linkedlifedata.com/resource/pubmed/id/17081365

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2006-11-3
pubmed:abstractText
Brugada syndrome is an inherited channelopathy that characterized by ST-segment elevation in the right precordial lead (V(1)-V(3)) on the electrocardiogram with or without right bundle branch block and related with high risk of sudden cardiac death and structurally normal hearts. The first and only gene linked to this disease is SCN5A, a gene encodes for alpha subunit of the cardiac sodium channel. The objective of this study is to explore SCN5A gene mutations in Chinese patients with Brugada syndrome.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0253-3758
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
616-9
pubmed:dateRevised
2011-10-17
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
[Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617].
pubmed:affiliation
Department of Cardiology Center, Tongren Hospital, Capital University of Medical Sciences, Beijing 100730, China.
pubmed:publicationType
Journal Article, English Abstract