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Autosomal recessive “uncomplicated” profound childhood deafness in an arabic family with high consanguinity

✍ Scribed by A. Kabarity; S. A. Al-Awadi; T. I. Farag; G. Mallalah


Book ID
104702650
Publisher
Springer
Year
1981
Tongue
English
Weight
296 KB
Volume
57
Category
Article
ISSN
0340-6717

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Recently the TMPRSS3 gene, which encodes a transmembrane serine protease, was found to be responsible for two non-syndromic recessive deafness loci located on human chromosome 21q22.3, DFNB8 and DFNB10. We found evidence for linkage to the DFNB8/10 locus in two unrelated consanguineous Tunisian fami