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New In Vitro Cellular Model for Molecular Studies of Retinitis Pigmentosa
Retinitis pigmentosa (RP) is an inherited form of retinal degeneration characterized by primary rod photoreceptor cell death followed by cone loss. Mutations in several genes linked to the disease cause increased levels of cyclic guanosine monophosphate (cGMP) and calcium ion influxes. The purpose o...
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| Vydáno v: | Int J Mol Sci |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8235468/ https://ncbi.nlm.nih.gov/pubmed/34208617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22126440 |
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