Genetic testing was completed on 1,294 persons with deafness referred to the Molecular Otolaryngology Research Laboratories to establish a diagnosis of DFNB1. Exon 2 of GJB2 was screened for coding sequence allele variants by denaturing high-performance liquid chromatography (DHPLC) complemented by
β¦ LIBER β¦
Low frequency of deafness-associated GJB2 variants in Kenya and Sudan and novel GJB2 variants
β Scribed by Nagla M.A. Gasmelseed; Martin Schmidt; Mubarak M.A. Magzoub; Muthure Macharia; Osman M. Elmustafa; Benson Ototo; Enno Winkler; Gerd Ruge; Rolf D. Horstmann; Christian G. Meyer
- Book ID
- 102264138
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 36 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1059-7794
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β¦ Synopsis
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