This locus, identified by homozygosity mapping, overlaps that of DFNA47. It may be that mutations of the same gene are responsible for recessive and dominant hearing loss. [provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DFNB83-20-RE | 20 (40 μL) | 200 μL |  |
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| DFNB83-20-OR | 20 (40 μL) | 200 μL |  |
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| DFNB83-20-GO | 20 (40 μL) | 200 μL |  |
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| DFNB83-20-GR | 20 (40 μL) | 200 μL |  |
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| DFNB83-20-AQ | 20 (40 μL) | 200 μL |  |
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This locus, identified by homozygosity mapping, overlaps that of DFNA47. It may be that mutations of the same gene are responsible for recessive and dominant hearing loss. [provided by RefSeq, Feb 2010]
Gene Symbol : DFNB83
Gene Name : Deafness, autosomal recessive 83
Chromosome : CHR 9: 0-0
Locus : 9p23-p21.2
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