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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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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2018
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| Assuntos: | |
| Acesso em linha: | 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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