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The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

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Description scientific article
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author: Gabriele Crimi  Arthur Wilde  Elena V. Zaklyazminskaya  Lia Crotti  Gaetano M. De Ferrari  Michael J Ackerman  Peter J. Schwartz 

Publication date November 5, 2007
Language English
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