Article
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
Human molecular genetics - 1 Jun 1994
Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C
Abstract excerpt
The identification of mouse models for the various forms of human neurosensory non-syndromic recessive deafness would constitute a major advance in the study of human deafness. Here we describe the localization of a human gene for neurosensory, nonsyndromic recessive deafness (NSRD2) to chromosom...
Topics
- Animals
- Base Sequence
- Chromosome Mapping
- Chromosomes, Artificial, Yeast
- Chromosomes, Human, Pair 11
- Consanguinity
- DNA
- DNA, Satellite
- Deafness
- Female
- Genes, Recessive
- Genetic Linkage
- Genetic Markers
- Genotype
- Homozygote
- Humans
- Lod Score
- Male