Miyajima, H., Moteki, H., Day, T., Nishio, S., Murata, T., Ikezono, T., . . . Usami, S. (2020). Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss. Sci Rep.
Citação norma ChicagoMiyajima, Hiroki, et al. "Novel ACTG1 Mutations in Patients Identified By Massively Parallel DNA Sequencing Cause Progressive Hearing Loss." Sci Rep 2020.
Citação norma MLAMiyajima, Hiroki, et al. "Novel ACTG1 Mutations in Patients Identified By Massively Parallel DNA Sequencing Cause Progressive Hearing Loss." Sci Rep 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.