Night blindness, congenital stationary

Known as: Congenital stationary night blindness, Congenital night blindness, Night blindness since birth 
A nonprogressive (i.e., stationary) form of difficulties with night blindness with congenital onset. [HPO:probinson]
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Night vision requires signaling from rod photoreceptors to adjacent bipolar cells in the retina. Mutations in the genes NYX and… (More)
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Highly Cited
2009
Highly Cited
2009
Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous group of retinal disorders… (More)
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Highly Cited
2000
Highly Cited
2000
During development, visual photoreceptors, bipolar cells and other neurons establish connections within the retina enabling the… (More)
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Highly Cited
1998
Highly Cited
1998
The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2) maps to a 1.1-Mb region in Xp11.23… (More)
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Highly Cited
1998
Highly Cited
1998
PURPOSE To clone and characterize the canine RPE65 cDNA from normal dog, examine for mutations, and establish if the mutation… (More)
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Highly Cited
1998
Highly Cited
1998
PURPOSE To describe a naturally occurring X-linked recessive mutation, no b-wave (nob), that compromises visual transmission… (More)
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Highly Cited
1993
Highly Cited
1993
A number of mutations in the rhodopsin gene have been shown to cause both dominant and recessive retinitis pigmentosa. Here we… (More)
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1989
1989
X-linked congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the… (More)
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Highly Cited
1986
Highly Cited
1986
An analysis of 64 patients with congenital stationary night blindness showed that all had essentially normal fundi… (More)
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Highly Cited
1983
Highly Cited
1983
Previous studies have reported that subjects affected with congenital stationary night blindness and myopia demonstrated some… (More)
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