Showing results 1 to 4 of 4
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Hearing loss: Frequency and functional studies of the most common connexin26 alleles Journal:Biochemical and Biophysical Research Communications | 2002 | ||
| 2003 | |||
Pathogenetic role of the deafness-related M34T mutation of Cx26 Journal:Human Molecular Genetics | 2006 | ||
Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease Journal:Neurobiology of Disease | 2006 |