Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics
淀粉样前体蛋白样蛋白2缺失诱导的视网膜突触病变与先天性静止性夜盲症相关:结构、功能和分子特征
期刊:Molecular Brain
影响因子:2.9
doi:10.1186/s13041-016-0245-z
Dinet, Virginie; Ciccotosto, Giuseppe D; Delaunay, Kimberley; Borras, Céline; Ranchon-Cole, Isabelle; Kostic, Corinne; Savoldelli, Michèle; El Sanharawi, Mohamed; Jonet, Laurent; Pirou, Caroline; An, Na; Abitbol, Marc; Arsenijevic, Yvan; Behar-Cohen, Francine; Cappai, Roberto; Mascarelli, Frédéric