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Entries: 1-3  
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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
Authors: Veerman, C. C.; Mengarelli, I.; Lodder, E. M.; Kosmidis, G.; Bellin, M.; Zhang, M.; Dittmann, S.; Guan, K.; Wilde, A. A. M.; Schulze-Bahr, E.; Greber, B.; Bezzina, C. R.; Verkerk, A. O.
Date of Publication (YYYY-MM-DD): 2017-07-24
Title of Journal: J am Heart Assoc
Volume: 6
Issue / Number: 7
Document Type: Article
ID: 744091.0
Reply to Christ et al.: LQT1 and JLNS phenotypes in hiPSC-derived cardiomyocytes are due to KCNQ1 mutations
Authors: Greber, B.; Verkerk, A. O.; Seebohm, G.; Mummery, C. L.; Bellin, M.
Date of Publication (YYYY-MM-DD): 2015-04-21
Title of Journal: Proc Natl Acad Sci u S A
Volume: 112
Issue / Number: 16
Start Page: E1969
Document Type: Article
ID: 717313.0
Human iPS cell models of Jervell and Lange-Nielsen syndrome
Authors: Bellin, M.; Greber, B.
Date of Publication (YYYY-MM-DD): 2015
Title of Journal: Rare Dis
Volume: 3
Issue / Number: 1
Start Page: e1012978
Document Type: Article
ID: 717326.0
Entries: 1-3  
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