Cargando...
SPATA7: Evolving Phenotype from Cone-Rod Dystrophy to Retinitis Pigmentosa
BACKGROUND: SPATA7 mutations have been associated with different autosomal recessive retinal degeneration phenotypes. Long-term follow-up has not been described in detail. MATERIALS AND METHODS: A Hispanic patient with SPATA7 mutations was evaluated serially over a 12-year period with kinetic and st...
Guardado en:
| Publicado en: | Ophthalmic Genet |
|---|---|
| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2016
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4988809/ https://ncbi.nlm.nih.gov/pubmed/26854980 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/13816810.2015.1130154 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|