A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.

Zhang, K

A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease. [electronic resource] - American journal of ophthalmology Dec 1999 - 720-4 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0002-9394

10.1016/s0002-9394(99)00236-6 doi


ATP-Binding Cassette Transporters--genetics
Adult
Base Sequence
Cohort Studies
DNA Mutational Analysis
Eye Diseases, Hereditary--genetics
Female
Fluorescein Angiography
Fundus Oculi
Humans
Macular Degeneration--genetics
Middle Aged
Molecular Sequence Data
Pedigree
Point Mutation
Polymorphism, Single-Stranded Conformational
Sequence Analysis, DNA
Visual Acuity