A carregar...
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...
Na minha lista:
| Publicado no: | JAMA Ophthalmol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|