Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00833.x/fullpdf
Reference32 articles.
1. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23;Bork;Am J Hum Genet,2001
2. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D;Bolz;Nat Genet,2001
3. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness;Astuto;Am J Hum Genet,2002
4. Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22;Chaib;Hum Mol Genet,1996
5. Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10;Wayne;Hum Mol Genet,1996
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