Bross, P., Naundrup, S., Hansen, J., Nielsen, M. N., Christensen, J. H., Kruhøffer, M., . . . Nielsen, K. L. (2008). The Hsp60-(p.V98I) Mutation Associated with Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Both in Vitro and in Vivo. American Society for Biochemistry and Molecular Biology.
Citação norma ChicagoBross, Peter, et al. The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Both in Vitro and In Vivo. American Society for Biochemistry and Molecular Biology, 2008.
MLA citiranjeBross, Peter, et al. The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Both in Vitro and In Vivo. American Society for Biochemistry and Molecular Biology, 2008.