congenital stationary night blindness type 3 (CSNB3)

Genetics

• autosomal dominant form associated with defects in GNAT1 (Gt-alpha)

More general terms

• congenital night blindness

Additional terms

• voltage-dependent Ca+2 channel alpha-1F (L type, Cav1.4, CACNA1F, CACNAF1)

Database

• OMIM: https://mirror.omim.org/entry/139330