Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2. [electronic resource]
Producer: 20141203Description: 514-23 p. digitalISSN:- 1933-6969
- Amino Acid Sequence
- Animals
- Calcium Channels -- deficiency
- Calcium Channels, L-Type
- Eye Diseases, Hereditary -- genetics
- Female
- Gene Knockout Techniques
- Genetic Diseases, X-Linked -- genetics
- HEK293 Cells
- Humans
- Male
- Mice
- Molecular Sequence Data
- Myopia -- genetics
- Night Blindness -- genetics
- Protein Transport
- Retinal Cone Photoreceptor Cells -- pathology
- Retinal Rod Photoreceptor Cells -- pathology
- Synapses -- metabolism
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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