A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00862.x/fullpdf
Reference18 articles.
1. Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations;Usami;Hum Genet,1999
2. Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese;Tsukamoto;Eur J Hum Genet,2003
3. Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations;Campbell;Hum Mutat,2001
4. Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness;Park;J Med Genet,2003
5. Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans;Park;Clin Genet,2005
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