Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa. [electronic resource]
Producer: 20051114Description: 1258-64 p. digitalISSN:- 0007-1161
- Adolescent
- Adult
- Age of Onset
- Amino Acid Sequence
- Child
- Child, Preschool
- DNA Mutational Analysis -- methods
- Female
- Genes, Dominant
- Genotype
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Mutation, Missense
- Pedigree
- Phenotype
- Polymorphism, Restriction Fragment Length
- Retinitis Pigmentosa -- genetics
- Rhodopsin -- genetics
- Visual Acuity
- Visual Fields
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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