Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

por Waldner, D. M., Giraldo Sierra, N. C., Bonfield, S., Nguyen, L., Dimopoulos, I. S., Sauvé, Y., Stell, W. K., Bech-Hansen, N. T.
Publicado 2018