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Zebrafish Cacna1fa is required for cone photoreceptor function and synaptic ribbon formation
Mutations in the human CACNA1F gene cause incomplete congenital stationary night blindness type 2 (CSNB2), a non-progressive, clinically heterogeneous retinal disorder. However, the molecular mechanisms underlying CSNB2 have not been fully explored. Here, we describe the positional cloning of a blin...
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| Главные авторы: | , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Oxford University Press
2014
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4014194/ https://ncbi.nlm.nih.gov/pubmed/24419318 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu009 |
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