Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

7 páginas, 2 figuras.

Bibliographic Details
Authors:	Martínez Mir, Amalia, Paloma, Eva, Allikmets, Rando, Ayuso, Carmen, Río, Teresa del, Dean, Michael, Vilageliu, L., González-Duarte, Roser, Balcells, Susanna
Format:	article
Publication Date:	1998
Country:	España
Institution:	Consejo Superior de Investigaciones Científicas (CSIC)
Repository:	DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:	oai:digital.csic.es:10261/39477
Online Access:	http://hdl.handle.net/10261/39477
Access Level:	Open access
Keyword:	ATP-binding cassette transporters Framshift mutation Homozygote Macular degeneration Pedigree Retinitis pigmentosa

Description
Summary:	7 páginas, 2 figuras.