Article
The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.
Genomics - 1 Jul 1991
Travis G H, Christerson L, Danielson P E, Klisak I, Sparkes R S, Hahn L B, Dryja T P, Sutcliffe J G
Abstract excerpt
Retinal degeneration slow (rds) is a mouse neurological mutation that is characterized phenotypically by abnormal development of rod and cone photoreceptors followed by their slow degeneration. This phenotype resembles the pathologic abnormalities seen in retinitis pigmentosa. The mouse rds gene...
Topics
- Amino Acid Sequence
- Animals
- Base Sequence
- Cattle
- Chromosome Mapping
- Chromosomes, Human, Pair 6
- Cricetinae
- Cricetulus
- DNA
- Disease Models, Animal
- Eye Proteins
- Genes
- Humans
- Hybrid Cells
- Intermediate Filament Proteins
- Membrane Glycoproteins
- Mice
- Molecular Sequence Data