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Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish
Mutations in eyes shut homolog (EYS), a gene predominantly expressed in the photoreceptor cells of the retina, are among the most frequent causes of autosomal recessive (ar) retinitis pigmentosa (RP), a progressive retinal disorder. Due to the absence of EYS in several rodent species and its retina-...
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| Publicat a: | PLoS One |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6063403/ https://ncbi.nlm.nih.gov/pubmed/30052645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0200789 |
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