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Abundant L-type calcium channel Ca(v)1.3 (α1D) subunit mRNA is detected in rod photoreceptors of the mouse retina via in situ hybridization
PURPOSE: Mutations in the CACNA1F gene encoding the L-type calcium channel pore-forming Ca(v)1.4 (α1F) subunit in humans result in an incomplete form of congenital stationary night blindness (CSNB2) with residual photoreceptor function. It has been postulated that this residual function, at least in...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Molecular Vision
2007
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768761/ https://www.ncbi.nlm.nih.gov/pubmed/17563731 |