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Localization of CHMP2B in postnatal rd1 mouse retina
Retinitis pigmentosa is the most common form of inherited blindness in humans. A well-studied model of the disease is the rd1 mouse, characterized by a loss of function mutation in the catalytic β subunit of the phosphodiesterase 6 (Pde6) holoenzyme involved in phototransduction within rods and cone...
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| Publicado no: | Bios |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6611702/ https://ncbi.nlm.nih.gov/pubmed/31281183 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1893/0005-3155-89.2.58 |
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