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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

Semantic Scholar uses AI to extract papers important to this topic.
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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