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Deciphering the pathogenic role of a variant with uncertain significance for short QT and Brugada syndromes using gene-edited human-induced pluripotent stem cell-derived cardiomyocytes and preclinical drug screening

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Item Type:Letter
Title:Deciphering the pathogenic role of a variant with uncertain significance for short QT and Brugada syndromes using gene-edited human-induced pluripotent stem cell-derived cardiomyocytes and preclinical drug screening
Creators Name:El-Battrawy, I., Lan, H., Cyganek, L., Maywald, L., Zhong, R., Zhang, F., Xu, Q., Lee, J., Duperrex, E., Hierlemann, A., Saguner, A.M., Duru, F., Kovacs, B., Huang, M., Liao, Z., Albers, S., Müller, J., Dinkel, H., Rose, L., Hohn, A., Yang, Z., Qiao, L., Li, Y., Lang, S., Kleinsorge, M., Mügge, A., Aweimer, A., Fan, X., Diecke, S., Akin, I., Li, G. and Zhou, X.
Keywords:Brugada Syndrome, Cardiac Death, Channelopathy, Short QT Syndrome
Source:Clinical and Translational Medicine
ISSN:2001-1326
Publisher:Wiley
Volume:11
Number:12
Page Range:e646
Date:26 December 2021
Official Publication:https://doi.org/10.1002/ctm2.646
PubMed:View item in PubMed

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