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NOS1AP Is a Genetic Modifier of Congenital Long-QT Syndrome

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Year: 2009
Type: article
Study design: Observational Study
Source: Heart Rhythm
DOI: 10.1016/j.hrthm.2009.09.058
Authors: Lia Crotti, Roberto Insolia, Maria Cristina Monti, Matteo Pedrazzini, Erika Taravelli, Anna Peljto, Althea Goosen, Paul A. Brink, David A. Greenberg, Peter J. Schwartz, Alfred L. George
Institutions: University of Pavia, Policlinico San Matteo Fondazione, Columbia University Irving Medical Center, Columbia University, Stellenbosch University, NewYork–Presbyterian Hospital, Vanderbilt University
Language: English

Topic: Cardiac electrophysiology and arrhythmias
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W1991580166
FWCI:
Cites:
Cited by: 1
Related to: 10
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