Photoreceptor Degeneration in Two Mouse Models for Congenital Stationary Night Blindness Type 2

Light-dependent conductance changes of voltage-gated Ca(v)1.4 channels regulate neurotransmitter release at photoreceptor ribbon synapses. Mutations in the human CACNA1F gene encoding the α1F subunit of Ca(v)1.4 channels cause an incomplete form of X-linked congenital stationary night blindness (CSN...

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Detalles Bibliográficos
Autores principales: Regus-Leidig, Hanna, Atorf, Jenny, Feigenspan, Andreas, Kremers, Jan, Maw, Marion A., Brandstätter, Johann Helmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897778/
https://www.ncbi.nlm.nih.gov/pubmed/24466230
http://dx.doi.org/10.1371/journal.pone.0086769

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897778/
https://www.ncbi.nlm.nih.gov/pubmed/24466230
http://dx.doi.org/10.1371/journal.pone.0086769

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