A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit. [electronic resource]
Producer: 20150109Description: e95768 p. digitalISSN:- 1932-6203
- Animals
- Animals, Genetically Modified
- Catalytic Domain -- genetics
- Cyclic Nucleotide Phosphodiesterases, Type 6 -- genetics
- Eye Diseases, Hereditary -- etiology
- Genetic Diseases, X-Linked -- etiology
- Heterotrimeric GTP-Binding Proteins -- genetics
- Humans
- Light Signal Transduction -- genetics
- Mutation
- Myopia -- etiology
- Night Blindness -- etiology
- Transducin
- Xenopus laevis
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.