Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F. [electronic resource]
Producer: 20091102Description: 174-9 p. digitalISSN:- 1878-0849
- Algeria
- Alleles
- Amino Acid Sequence
- Audiometry
- Binding Sites
- Cadherin Related Proteins
- Cadherins -- genetics
- Case-Control Studies
- Connexin 26
- Connexin 30
- Connexins -- genetics
- Consanguinity
- Deafness -- diagnosis
- Genetic Heterogeneity
- Genetic Variation
- Genotype
- Haplotypes
- Homozygote
- Humans
- Models, Molecular
- Molecular Sequence Data
- Mutation
- Protein Binding
- Protein Structure, Tertiary
- Sequence Homology, Amino Acid
- Usher Syndromes -- genetics
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.