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Cone Structure in Patients With Usher Syndrome Type III and Mutations in the Clarin 1 Gene
OBJECTIVE: To study macular structure and function in patients with Usher syndrome type III (USH3) caused by mutations in the Clarin 1 gene (CLRN1). METHODS: High-resolution macular images were obtained by adaptive optics scanning laser ophthalmoscopy and spectral domain optical coherence tomography...
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| Publicado en: | JAMA Ophthalmol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4482614/ https://ncbi.nlm.nih.gov/pubmed/22964989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/2013.jamaophthalmol.2 |
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