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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

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.

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 Creators:
Veerman, Christiaan C.1, Author
Mengarelli, Isabella1, Author
Lodder, Elisabeth M.1, Author
Kosmidis, Georgios1, Author
Bellin, Milena1, Author
Zhang, Miao2, Author           
Dittmann, Sven1, Author
Guan, Kaomei1, Author
Wilde, Arthur A.M.1, Author
Schulze-Bahr, Eric1, Author
Greber, Boris2, Author           
Bezzina, Connie R.1, Author
Verkerk, Arie O.1, Author
Affiliations:
1External Organizations, ou_persistent22              
2Chemical Genomics Center of the MPS, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753292              

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Free keywords: arrhythmia (heart rhythm disorders) • sodium channels • stem cell
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Language(s): eng - English
 Dates: 2017-07-24
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1161/JAHA.116.005135
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Title: Journal of the American Heart Association
Source Genre: Journal
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Pages: - Volume / Issue: 6 (7) Sequence Number: - Start / End Page: 1 - 21 Identifier: -