Retinoid Binding Properties of Nucleotide Binding Domain 1 of the Stargardt Disease-associated ATP Binding Cassette (ABC) Transporter, ABCA4

Author:

Biswas-Fiss Esther E.,Affet Stephanie,Ha Malissa,Biswas Subhasis B.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference70 articles.

1. The ABCR gene in recessive and dominant Stargardt diseases. A genetic pathway in macular degeneration;Zhang;Genomics,1999

2. The gene for Stargardt disease, ABCA4, is a major retinal gene. A mini-review;Koenekoop;Ophthalmic Genet.,2003

3. A novel ABCR nonsense mutation responsible for late-onset fundus flavimaculatus;Souied;Invest. Ophthalmol. Vis. Sci.,1999

4. An analysis of ABCR mutations in British patients with recessive retinal dystrophies;Papaioannou;Invest. Ophthalmol. Vis. Sci.,2000

5. Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus;Lois;Invest. Ophthalmol. Vis. Sci.,1999

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