Showing results 1 to 3 of 3
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness Journal:Cell Communication and Adhesion | 2001 | ||
Hearing loss: Frequency and functional studies of the most common connexin26 alleles Journal:Biochemical and Biophysical Research Communications | 2002 | ||
| 2003 |