Amiott, E. A., Cohen, M. M., Saint-Georges, Y., Weissman, A. M., & Shaw, J. M. (2009). A Mutation Associated with CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover. The American Society for Cell Biology.
Chicago-tyylinen lähdeviittausAmiott, Elizabeth A., Mickael M. Cohen, Yann Saint-Georges, Allan M. Weissman, ja Janet M. Shaw. A Mutation Associated With CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover. The American Society for Cell Biology, 2009.
MLA-viiteAmiott, Elizabeth A., et al. A Mutation Associated With CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover. The American Society for Cell Biology, 2009.
Varoitus: Nämä viitteet eivät aina ole täysin luotettavia.