Dinet, V., Ciccotosto, G. D., Delaunay, K., Borras, C., Ranchon-Cole, I., Kostic, C., . . . Mascarelli, F. (2016). Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: Structural, functional and molecular characteristics. Mol Brain.
Citação norma ChicagoDinet, Virginie, et al. "Amyloid Precursor-Like Protein 2 Deletion-induced Retinal Synaptopathy Related to Congenital Stationary Night Blindness: Structural, Functional and Molecular Characteristics." Mol Brain 2016.
Citação norma MLADinet, Virginie, et al. "Amyloid Precursor-Like Protein 2 Deletion-induced Retinal Synaptopathy Related to Congenital Stationary Night Blindness: Structural, Functional and Molecular Characteristics." Mol Brain 2016.