Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array. [electronic resource]
Producer: 20100820Description: 3884-92 p. digitalISSN:- 1552-5783
- Adolescent
- Adult
- Amino Acid Sequence
- Child
- Child, Preschool
- Chromosome Mapping
- Color Perception Tests
- Color Vision Defects -- genetics
- Cone Opsins -- genetics
- DNA Mutational Analysis
- Electroretinography
- Female
- Genes, X-Linked
- Genetic Diseases, X-Linked -- genetics
- Heterozygote
- Humans
- Jews -- genetics
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Nystagmus, Pathologic -- genetics
- Pedigree
- Phenotype
- Retinal Degeneration -- genetics
- Tomography, Optical Coherence
- Visual Acuity -- physiology
- Visual Fields
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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