Skip to search form
Skip to main content
Semantic Scholar
All Fields
All Fields
Art
Biology
Business
Computer Science
Chemistry
Economics
Engineering
Environmental Science
Geography
Geology
History
Materials Science
Mathematics
Medicine
Philosophy
Physics
Political Science
Psychology
Sociology
FAQ
Contact Us
•
Sign In
Create Free Account
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2
Known as:
CSNBAD2
, NIGHT BLINDNESS, CONGENITAL STATIONARY, RAMBUSCH TYPE
National Institutes of Health
Watch Topic
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.
Kota N. Gopalakrishna
,
Kimberly K. Boyd
,
Nikolai O Artemyev
Cellular signalling
2017
Mutations in PDE6 genes encoding the effector enzymes in rods and cones underlie severe retinal diseases including retinitis…
Expand
Is this relevant?