Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem 
Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction 
Disease-Causing Mutation

Veerman, Christiaan C.; Mengarelli, Isabella; Lodder, Elisabeth M.; Kosmidis, Georgios; Bellin, Milena; Zhang, Miao; Dittmann, Sven; Guan, Kaomei; Wilde, Arthur A.M.; Schulze-Bahr, Eric; Greber, Boris; Bezzina, Connie R.; Verkerk, Arie O.

doi:10.1161/JAHA.116.005135

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Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation

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Zhang, Miao
Chemical Genomics Center of the MPS, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Greber, Boris
Chemical Genomics Center of the MPS, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Veerman, C. C., Mengarelli, I., Lodder, E. M., Kosmidis, G., Bellin, M., Zhang, M., et al. (2017). Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing Mutation. Journal of the American Heart Association, 6(7), 1-21. doi:10.1161/JAHA.116.005135.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-A687-2

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