Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene.

Klevering, B J

Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene. [electronic resource] - The British journal of ophthalmology Aug 1999 - 914-8 p. digital

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

0007-1161

10.1136/bjo.83.8.914 doi


ATP-Binding Cassette Transporters--genetics
Adult
Aged
Aged, 80 and over
Consanguinity
Female
Genotype
Humans
Male
Middle Aged
Mutation--genetics
Night Blindness--genetics
Pedigree
Phenotype
Retinal Degeneration--genetics
Visual Acuity--genetics
Visual Fields--genetics