The spectrum of human rhodopsin disease mutations through the lens of interspecific variation. [electronic resource]
Producer: 20040824Description: 107-18 p. digitalISSN:- 0378-1119
- Amino Acid Sequence
- Amino Acid Substitution
- Animals
- Codon -- genetics
- Conserved Sequence -- genetics
- Evolution, Molecular
- Gene Frequency
- Genetic Variation
- Genotype
- Humans
- Molecular Sequence Data
- Mutation
- Phenotype
- Phylogeny
- Retinal Diseases -- genetics
- Retinitis Pigmentosa -- genetics
- Rhodopsin -- genetics
- Species Specificity
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.