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The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2.
scientific article published on 12 April 2017
Author/s
author: Maria Chiara Ciuffreda, Rita Zappatore, Federica Pisano, Lia Crotti, Massimiliano Gnecchi, Peter J. Schwartz
Work details
Publication date
April 12, 2017
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Language
English
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