Salvarani, N.; Peretto, G.; Silvia, C.; Villatore, A.; Thairi, C.; Santoni, A.; Galli, C.; Carrera, P.; Sala, S.; Benedetti, S.;
et al. Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. Int. J. Mol. Sci. 2023, 24, 9548.
https://doi.org/10.3390/ijms24119548
AMA Style
Salvarani N, Peretto G, Silvia C, Villatore A, Thairi C, Santoni A, Galli C, Carrera P, Sala S, Benedetti S,
et al. Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. International Journal of Molecular Sciences. 2023; 24(11):9548.
https://doi.org/10.3390/ijms24119548
Chicago/Turabian Style
Salvarani, Nicolò, Giovanni Peretto, Crasto Silvia, Andrea Villatore, Cecilia Thairi, Anna Santoni, Camilla Galli, Paola Carrera, Simone Sala, Sara Benedetti,
and et al. 2023. "Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells" International Journal of Molecular Sciences 24, no. 11: 9548.
https://doi.org/10.3390/ijms24119548
APA Style
Salvarani, N., Peretto, G., Silvia, C., Villatore, A., Thairi, C., Santoni, A., Galli, C., Carrera, P., Sala, S., Benedetti, S., Di Pasquale, E., & Di Resta, C.
(2023). Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. International Journal of Molecular Sciences, 24(11), 9548.
https://doi.org/10.3390/ijms24119548
