Showing results 1 to 6 of 6
| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Connexin32 in the peripheral nervous system: Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease Journal:Annals of the New York Academy of Sciences | 1999 | 127 | ||
Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness Journal:Cell Communication and Adhesion | 2001 | 209 | ||
Hearing loss: Frequency and functional studies of the most common connexin26 alleles Journal:Biochemical and Biophysical Research Communications | 2002 | 174 | ||
| 2003 | 186 | |||
Pathogenetic role of the deafness-related M34T mutation of Cx26 Journal:Human Molecular Genetics | 2006 | 193 | ||
Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease Journal:Neurobiology of Disease | 2006 | 186 |