Tom Rossenbacker - JoVE Visualize

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Human Mutation|April 4, 2003

A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gatingXander H T Wehrens, Tom Rossenbacker, Roselie J Jongbloed, et al.

Journal of Molecular Medicine (Berlin, Germany)|November 20, 2004

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?Jop H van Berlo, Willem G de Voogt, Anneke J van der Kooi, et al.

American Heart Journal|November 24, 2007

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinicsJ Peter van Tintelen, Robert M W Hofstra, Hilga Katerberg, et al.

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Showing results (11-20 of 13) with videos related to

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Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Human Mutation|April 4, 2003

A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gatingXander H T Wehrens, Tom Rossenbacker, Roselie J Jongbloed, et al.

Journal of Molecular Medicine (Berlin, Germany)|November 20, 2004

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?Jop H van Berlo, Willem G de Voogt, Anneke J van der Kooi, et al.

American Heart Journal|November 24, 2007

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinicsJ Peter van Tintelen, Robert M W Hofstra, Hilga Katerberg, et al.

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