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Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse
Mutations in the elongation of very long chain fatty acid 4 (ELOVL4) gene cause Stargardt macular dystrophy 3 (STGD3), a rare, juvenile-onset, autosomal dominant form of macular degeneration. Although several mouse models have already been generated to investigate the link between the three identifi...
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| Publié dans: | PLoS One |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Public Library of Science
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5749830/ https://ncbi.nlm.nih.gov/pubmed/29293603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0190514 |
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