Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2. [electronic resource]
- Channels (Austin, Tex.)
- 514-23 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1933-6969
10.4161/chan.26376 doi
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