Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.nature.com/articles/gt201359.pdf
Reference42 articles.
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2. Smith RJ, Bale JF Jr, White KR . Sensorineural hearing loss in children. Lancet 2005; 365: 879–890.
3. Dror AA, Avraham KB . Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet 2009; 43: 411–437.
4. Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR et al. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet 1997; 6: 2173–2177.
5. Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R et al. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. N Engl J Med 1998; 339: 1500–1505.
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