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Mutation analysis of the Cx26 , Cx30 , and Cx31 genes in autosomal recessive nonsyndromic hearing impairment

✍ Scribed by Gürtler, Nicolas; Egenter, Carole; Bösch, Nemya; Plasilova, Martina


Book ID
119939469
Publisher
Informa plc
Year
2008
Tongue
English
Weight
197 KB
Volume
128
Category
Article
ISSN
0001-6489

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Mutations in the Cx26 gene have been shown to cause autosomal recessive nonsyndromic hearing loss (ARNSHL) at the DFNB1 locus on chromosome 13q12. Using direct sequencing, we screened the Cx26 coding region of affected and nonaffected members from seven ARNSHL families either linked to the DFNB1 loc