Di Stefano, M., Loreto, A., Orsomando, G., Mori, V., Zamporlini, F., Hulse, R. P., . . . Conforti, L. (2017). NMN deamidase delays Wallerian degeneration and rescues axonal defects caused by NMNAT2 deficiency in vivo. Elsevier (Cell Press).
Chicago Style (17th ed.) CitationDi Stefano, Michele, et al. NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency in Vivo. Elsevier (Cell Press), 2017.
MLA (9th ed.) CitationDi Stefano, Michele, et al. NMN Deamidase Delays Wallerian Degeneration and Rescues Axonal Defects Caused by NMNAT2 Deficiency in Vivo. Elsevier (Cell Press), 2017.
Warning: These citations may not always be 100% accurate.