Cita APA (7a ed.)

Salvarani, N., Crasto, S., Miragoli, M., Bertero, A., Paulis, M., Kunderfranco, P., . . . Pasquale, E. D. (2019). The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy. Nature Portfolio.

Cita Chicago Style (17a ed.)

Salvarani, Nicolò, et al. The K219T-Lamin Mutation Induces Conduction Defects Through Epigenetic Inhibition of SCN5A in Human Cardiac Laminopathy. Nature Portfolio, 2019.

Cita MLA (8a ed.)

Salvarani, Nicolò, et al. The K219T-Lamin Mutation Induces Conduction Defects Through Epigenetic Inhibition of SCN5A in Human Cardiac Laminopathy. Nature Portfolio, 2019.