Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Dinet V., Ciccotosto G.D., Delaunay K., Borras C., Ranchon-Cole I., Kostic C., Savoldelli M., El Sanharawi M., Jonet L., Pirou C. et al., 2016/06/08. Molecular brain, 9 (1) p. 64. Peer-reviewed.
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