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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


Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Authors: Horn, D.; Kapeller, J.; Rivera-Brugues, N.; Moog, U.; Lorenz-Depiereux, B.; Eck, S.; Hempel, M.; Wagenstaller, J.; Gawthrope, A.; Monaco, A. P.; Bonin, M.; Riess, O.; Wohlleber, E.; Illig, T.; Bezzina, C. R.; Franke, A.; Spranger, S.; Villavicencio-Lorini, P.; Seifert, W.; Rosenfeld, J.; Klopocki, E.; Rappold, G. A.; Strom, T. M.
Date of Publication (YYYY-MM-DD): 2010-11-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 11
Start Page: E1851
End Page: E1860
Document Type: Article
ID: 539476.0