night-blind

adj.

患夜盲症的；

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness.
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night...
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
A naturally occurring mouse model of X-linked congenital stationary night blindness.
The Briard dog: a new animal model of congenital stationary night blindness.
Congenital stationary night blindness with negative electroretinogram. A new classification
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness