Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. [electronic resource]
Producer: 20011018Description: 673-84 p. digitalISSN:- 0002-9297
- Abnormalities, Multiple -- genetics
- Base Sequence
- Chromosomes, Human, Pair 3 -- genetics
- Cloning, Molecular
- Contig Mapping
- Deafness -- genetics
- Expressed Sequence Tags
- Female
- Finland
- Founder Effect
- Gene Expression Profiling
- Genetic Linkage -- genetics
- Haplotypes -- genetics
- Humans
- Linkage Disequilibrium -- genetics
- Male
- Membrane Proteins -- chemistry
- Molecular Sequence Data
- Mutation -- genetics
- Pedigree
- Protein Structure, Secondary
- Protein Structure, Tertiary
- RNA, Messenger -- analysis
- Retina -- metabolism
- Retinal Degeneration -- genetics
- Syndrome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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