A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3. [electronic resource]
Producer: 20190524Description: 6102-6110 p. digitalISSN:- 1552-5783
- Animals
- Color Vision Defects -- genetics
- Cyclic Nucleotide-Gated Cation Channels -- genetics
- Dark Adaptation -- physiology
- Disease Models, Animal
- Electroretinography
- Exons -- genetics
- Female
- Genotyping Techniques
- Male
- Mice
- Mice, Inbred C57BL
- Mutation, Missense -- genetics
- Ophthalmoscopy
- Polymorphism, Restriction Fragment Length
- RNA, Messenger -- genetics
- Real-Time Polymerase Chain Reaction
- Retina -- physiopathology
- Retinal Cone Photoreceptor Cells -- pathology
- Tomography, Optical Coherence
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.