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- Title
Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.
- Authors
Rozet, J M; Gerber, S; Souied, E; Perrault, I; Châtelin, S; Ghazi, I; Leowski, C; Dufier, J L; Munnich, A; Kaplan, J
- Abstract
Stargardt disease (STGD) and late-onset fundus flavimaculatus (FFM) are autosomal recessive conditions leading to macular degenerations in childhood and adulthood, respectively. Recently, mutations of the photoreceptor cell-specific ATP binding transporter gene (ABCR) have been reported in Stargardt disease. Here, we report on the screening of the whole coding sequence of the ABCR gene in 40 unrelated STGD and 15 FFM families and we show that mutations truncating the ABCR protein consistently led to STGD. Conversely, all mutations identified in FFM were missense mutations affecting uncharged amino acids. These results provide the first genotype-phenotype correlations in ABCR gene mutations.
- Publication
European journal of human genetics : EJHG, 1998, Vol 6, Issue 3, p291
- ISSN
1018-4813
- Publication type
Journal Article
- DOI
10.1038/sj.ejhg.5200221