Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2

Mutations in the gene encoding Ca(v)1.4, CACNA1F(,) are associated with visual disorders including X-linked incomplete congenital stationary night blindness type 2 (CSNB2). In mice lacking Ca(v)1.4 channels, there are defects in the development of “ribbon” synapses formed between photoreceptors (PRs...

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Detalles Bibliográficos
Autores principales: Liu, Xiaoni, Kerov, Vasily, Haeseleer, Françoise, Majumder, Anurima, Artemyev, Nikolai, Baker, Sheila A, Lee, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042486/
https://www.ncbi.nlm.nih.gov/pubmed/24064553
http://dx.doi.org/10.4161/chan.26376

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042486/
https://www.ncbi.nlm.nih.gov/pubmed/24064553
http://dx.doi.org/10.4161/chan.26376

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