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NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2

Known as: CSNBAD2, NIGHT BLINDNESS, CONGENITAL STATIONARY, RAMBUSCH TYPE 
 
National Institutes of Health

Related topics

Related topics

4 relations

Broader (2)

Eye Diseases, HereditaryNight Blindness
HemeralopiaPDE6B gene

Papers overview

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2017
2017
Mechanisms of mutant PDE6 proteins underlying retinal diseases.
Mutations in PDE6 genes encoding the effector enzymes in rods and cones underlie severe retinal diseases including retinitis… Expand
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