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Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinic.

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Title: Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinic.
Authors: Gray C; Division of Cardiology, University of Western Ontario, London, Ontario, Canada., Gula LJ, Klein GJ, Skanes AC, Yee R, Sy R, Salisbury BA, Wong J, Chattha I, Subbiah RN, Krahn AD
Source: Journal of cardiovascular electrophysiology [J Cardiovasc Electrophysiol] 2010 Mar; Vol. 21 (3), pp. 296-300. Date of Electronic Publication: 2009 Oct 08.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Blackwell Country of Publication: United States NLM ID: 9010756 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-8167 (Electronic) Linking ISSN: 10453873 NLM ISO Abbreviation: J Cardiovasc Electrophysiol Subsets: MEDLINE
Database: MEDLINE Ultimate
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DbLabel: MEDLINE Ultimate
An: 19817925
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinic.
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  Data: <searchLink fieldCode="JN" term="%229010756%22">Journal of cardiovascular electrophysiology</searchLink> [J Cardiovasc Electrophysiol] 2010 Mar; Vol. 21 (3), pp. 296-300. <i>Date of Electronic Publication: </i>2009 Oct 08.
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  Data: Journal Article; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Blackwell%22">Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9010756 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1540-8167 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210453873%22">10453873 </searchLink><i>NLM ISO Abbreviation: </i>J Cardiovasc Electrophysiol <i>Subsets: </i>MEDLINE
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        Value: 10.1111/j.1540-8167.2009.01626.x
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        Text: English
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        StartPage: 296
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      – TitleFull: Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinic.
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              Text: 2010 Mar
              Type: published
              Y: 2010
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