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NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2

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

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2017
2017
Mutations in PDE6 genes encoding the effector enzymes in rods and cones underlie severe retinal diseases including retinitis… Expand
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