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Heart Rhythm
Volume 2, Issue 11
, Pages 1238-1249
, November 2005
Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome
References
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This work was supported by The John and Birthe Meyer Foundation, The Velux Foundation, The NovoNordisk Foundation, The Danish Heart Foundation, and The Beckett Foundation.
PII: S1547-5271(05)01890-4
doi: 10.1016/j.hrthm.2005.07.025
© 2005 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.
« Previous
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Heart Rhythm
Volume 2, Issue 11
, Pages 1238-1249
, November 2005
