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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3897778/ https://ncbi.nlm.nih.gov/pubmed/24466230 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0086769 |
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