Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies.
Ophthalmology
; 125(6): 894-903, 2018 06.
Article
en En
| MEDLINE
| ID: mdl-29398085
Texto completo:
1
Base de datos:
MEDLINE
Asunto principal:
Amaurosis Congénita de Leber
/
Mutación
/
Antígenos de Neoplasias
/
Proteínas de Neoplasias
Tipo de estudio:
Diagnostic_studies
/
Observational_studies
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Prognostic_studies
/
Risk_factors_studies
Idioma:
En
Revista:
Ophthalmology
Año:
2018
Tipo del documento:
Article