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NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
, NIGHT BLINDNESS, CONGENITAL STATIONARY, RAMBUSCH TYPE
National Institutes of Health
Eye Diseases, Hereditary
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Mechanisms of mutant PDE6 proteins underlying retinal diseases.
K. N. Gopalakrishna
Kimberly K. Boyd
Corpus ID: 6334418
Mutations in PDE6 genes encoding the effector enzymes in rods and cones underlie severe retinal diseases including retinitis…
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