Portal de investigación
Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Gamundi MJ
- Hernan I
- Maseras M
- Baiget M
- Borrego S
- Antiñolo G
- Valverde D
- Carballo M
Abstract
Only one mutation in the retinal fascin gene (FSCN2) has so far been associated with autosomal dominant retinitis pigmentosa (adRP) and macular dystrophy (adMD), in a Japanese population. Our study was designed to identify mutations in the FSCN2 gene among Spanish persons with adRP or adMD.
Datos de la publicación
- ISSN/ISSNe:
- 1090-0535, 1090-0535
- Tipo:
- Article
- Páginas:
- 922-928
- PubMed:
- 16280978
- Factor de Impacto:
- 1,164 SCImago ℠
- Cuartil:
- Q1 SCImago ℠
MOLECULAR VISION MOLECULAR VISION
Citas Recibidas en Web of Science: 13
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Cita
Gamundi MJ,Hernan I,Maseras M,Baiget M,AYUSO C,Borrego S,Antiñolo G,MILLÁN JM,Valverde D,Carballo M. Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration. Mol Vis. 2005. 11. (108-10):p. 922-928. IF:2,000. (1).