| Genetics of heart failure and sudden death. | |
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MedLine Citation:
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PMID: 20869650 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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Since the sentinel discovery of long QT syndrome as a channelopathy in 1995, many significant strides have been made related to exposing the pathogenic mechanisms underlying sudden cardiac death. However, elucidating the most influential genetic and environmental determinants that underlie the variable penetrance and expressivity of the primary syndrome-associated mutation remains a daunting task. |
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Authors:
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Matteo Vatta; Michael J Ackerman |
Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Heart failure clinics Volume: 6 ISSN: 1551-7136 ISO Abbreviation: Heart Fail Clin Publication Date: 2010 Oct |
Date Detail:
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Created Date: 2010-09-27 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101231934 Medline TA: Heart Fail Clin Country: United States |
Other Details:
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Languages: eng Pagination: 507-14, ix Citation Subset: IM |
Copyright Information:
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Copyright © 2010 Elsevier Inc. All rights reserved. |
Affiliation:
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Department of Pediatrics Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX 77030, USA. mvatta@bcm.edu |
Export Citation:
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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