A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome
| Author | K Kahrizi | en |
| Author | C Nishimura | en |
| Author | A Naghavi | en |
| Author | Y Riazalhosseini | en |
| Author | RJH Smith | en |
| Author | H Najmabadi | en |
| Issued Date | 2005-04-30 | en |
| Abstract | In the diagnosis of Pendred syndrome, assessment of individuals by molecular analysis of the SLC26A4 gene is recommended. Here we report a novel mutation in the SLC26A4 gene as revealed by denaturing high performance liquid chromatography (DHPLC) and DNA sequencing of the entire coding region of the SLC26A4 gene in five members of an Iranian family affected with Pendred syndrome. This is the first report of the molecular investigation of Pendred syndrome in Iran and the first report of the R79X mutation. | en |
| DOI | https://doi.org/ | en |
| Keyword | Pendred syndrome | en |
| Keyword | congenital deafness | en |
| Keyword | SLC26A4 | en |
| Keyword | R79X | en |
| Keyword | mutation analysis | en |
| Keyword | Iran Introduction | en |
| Publisher | Brieflands | en |
| Title | A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome | en |
| Type | Research Article | en |