Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis. [electronic resource]
Producer: 20060413Description: 263-73 p. digitalISSN:- 1090-0535
- Amino Acid Sequence
- Animals
- Base Sequence
- Blindness -- congenital
- Brain -- metabolism
- Carrier Proteins -- genetics
- Chromosomes, Human, Pair 9 -- genetics
- DNA Mutational Analysis
- Gene Expression Regulation -- physiology
- Genetic Variation
- Humans
- In Situ Hybridization
- Kidney -- metabolism
- Membrane Proteins -- genetics
- Mice
- Mice, Inbred CBA
- Molecular Sequence Data
- Mutation
- Open Reading Frames
- Polymorphism, Single-Stranded Conformational
- RNA, Messenger -- metabolism
- Retina -- metabolism
- Retinitis Pigmentosa -- genetics
- Reverse Transcriptase Polymerase Chain Reaction
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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