Article
Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA.
Experimental eye research - 1 Jul 1990
Cotran P R, Ringens P J, Crabb J W, Berson E L, Dryja T P
Abstract excerpt
We used a cDNA fragment corresponding to the human cellular retinaldehyde binding protein (CRALBP) gene to search for mutations at this locus in patients with autosomal dominant, autosomal recessive, or isolate retinitis pigmentosa, and Usher's syndrome, type I. No gene deletions or rearrangement...
Topics
- Alleles
- Carrier Proteins
- DNA
- Female
- Humans
- Male
- Mutation
- Pedigree
- Polymorphism, Restriction Fragment Length
- Retinaldehyde
- Retinitis Pigmentosa