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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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Related topics
Related topics
4 relations
Broader (2)
Eye Diseases, Hereditary
Night Blindness
Hemeralopia
PDE6B gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Mechanisms of mutant PDE6 proteins underlying retinal diseases.
K. Gopalakrishna
,
Kimberly K. Boyd
,
N. Artemyev
Cellular Signalling
2017
Corpus ID: 6334418
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