Identities, frequencies and origins ofTMC1mutations causing DFNB7/B11 deafness in Pakistan
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00895.x/fullpdf
Reference18 articles.
1. Autosomal and X-Linked Auditory Disorders
2. Human nonsyndromic sensorineural deafness;Friedman;Annu Rev Genomics Hum Genet,2003
3. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function;Kurima;Nat Genet,2002
4. Mutation screening of TMC1 in DFNB7/11 families;Yang;Am J Hum Genet,2002
5. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36;Vreugde;Nat Genet,2002
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