Article
Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin.
Human molecular genetics - 1 Jun 1993
Kranich H, Bartkowski S, Denton M J, Krey S, Dickinson P, Duvigneau C, Gal A
Abstract excerpt
No abstract is available from the source.
Topics
- Amino Acid Sequence
- Base Sequence
- Female
- Genes, Dominant
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Pedigree
- Phenotype
- Point Mutation
- Retinitis Pigmentosa
- Rhodopsin
