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E. Wilcox
Laboratory of Molecular Genetics
5 Research Court
NIDCD/NIH
Rockville
USA
Name/email consistency: high
- Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. Wilcox, E.R., Burton, Q.L., Naz, S., Riazuddin, S., Smith, T.N., Ploplis, B., Belyantseva, I., Ben-Yosef, T., Liburd, N.A., Morell, R.J., Kachar, B., Wu, D.K., Griffith, A.J., Riazuddin, S., Friedman, T.B. Cell (2001)
- Some deafness-causing mutations can be silenced with the appropriate gene partner. Wilcox, E., Riazuddin, S., Riazuddin, S. ScientificWorldJournal (2001)
- The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4. Wilcox, E.R., Everett, L.A., Li, X.C., Lalwani, A.K., Green, E.D. Adv. Otorhinolaryngol. (2000)
