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Screening of SLC26A4 gene in autoimmune thyroid diseases

✍ Scribed by Kallel, R.; Niasme-Grare, M.; Belguith-Maalej, S.; Mnif, M.; Abid, M.; Ayadi, H.; Masmoudi, S.; Jonard, L.; Hadj Kacem, H.

Book ID
121704639
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
167 KB
Volume
40
Category
Article
ISSN
1744-3121

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## Objectives: Mutations in the slc26a4 gene (7q22.3-7q31.1) are considered one of the most common causes of genetic hearing loss. there are two clinical forms related to these mutations: syndromic and non-syndromic deafness. the first one is named pendred syndrome (ps) when deafness is associated