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S-opsin knockout mice with the endogenous M opsin gene replaced by an L opsin variant
Specific variants of human long-wavelength (L) and middle-wavelength (M) cone opsin genes have recently been associated with a variety of vision disorders caused by cone malfunction, including red-green color vision deficiency, blue cone monochromacy, myopia, and cone dystrophy. Strikingly, unlike d...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4167788/ https://ncbi.nlm.nih.gov/pubmed/24801621 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0952523813000515 |
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