Portal de investigación
Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.
Fecha de publicación:
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Bernal S
- Avila-Fernández A
- Barragán I
- Baiget M
- Antiñolo G
- Külm M
Abstract
The purpose of this study was to test the ability of the genotyping microarray for Usher syndrome (USH) to identify the mutations responsible for the disease in a cohort of 183 patients with USH.
Datos de la publicación
- ISSN/ISSNe:
- 0146-0404, 1552-5783
- Tipo:
- Article
- Páginas:
- 1311-1317
- DOI:
- 10.1167/iovs.09-4085
- PubMed:
- 19683999
- Factor de Impacto:
- 2,038 SCImago ℠
- Cuartil:
- Q1 SCImago ℠
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Citas Recibidas en Web of Science: 57
Documentos
- No hay documentos
Filiaciones
Cita
JAIJO T,ALLER E,GARCÍA G,APARISI MJ,Bernal S,Avila A,Barragán I,Baiget M,AYUSO C,Antiñolo G,DÍAZ M,Külm M,BENEYTO M,NÁJERA C,MILLÁN JM. Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. Invest. Ophthalmol. Vis. Sci. 2010. 51. (3):p. 1311-1317. IF:3,466. (1).