Cite
Effective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathy.
MLA
Di Meo, Ivano, et al. “Effective AAV-Mediated Gene Therapy in a Mouse Model of Ethylmalonic Encephalopathy.” EMBO Molecular Medicine, vol. 4, no. 9, Sept. 2012, pp. 1008–14. EBSCOhost, https://doi.org/10.1002/emmm.201201433.
APA
Di Meo, I., Auricchio, A., Lamperti, C., Burlina, A., Viscomi, C., & Zeviani, M. (2012). Effective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathy. EMBO Molecular Medicine, 4(9), 1008–1014. https://doi.org/10.1002/emmm.201201433
Chicago
Di Meo, Ivano, Alberto Auricchio, Costanza Lamperti, Alberto Burlina, Carlo Viscomi, and Massimo Zeviani. 2012. “Effective AAV-Mediated Gene Therapy in a Mouse Model of Ethylmalonic Encephalopathy.” EMBO Molecular Medicine 4 (9): 1008–14. doi:10.1002/emmm.201201433.