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.
MLA CitationMiyajima, Hiroki, et al. "Novel ACTG1 Mutations in Patients Identified By Massively Parallel DNA Sequencing Cause Progressive Hearing Loss." Sci Rep 2020.
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