| Title | Author(s) | Year | View Count |
 | 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 | Nicholson, SM; Ressot, C; Gomès, D; D'Andrea, P; Perea, J; Duval, N; Bruzzone, R | 1999 | 80 |
| Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness | Bruzzone, R; Gomès, D; Denoyelle, F; Duval, N; Perea, J; Veronesi, V; Weil, D; Petit, C; Gabellec, MM; D'Andrea, P; White, TW | 2001 | 140 |
| Hearing loss: Frequency and functional studies of the most common connexin26 alleles | D'Andrea, P; Veronesi, V; Bicego, M; Melchionda, S; Zelante, L; Di Iorio, E; Bruzzone, R; Gasparini, P | 2002 | 109 |
| Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness | Bruzzone, R; Veronesi, V; Gomès, D; Bicego, M; Duval, N; Marlin, S; Petit, C; D'Andrea, P; White, TW | 2003 | 134 |
| Pathogenetic role of the deafness-related M34T mutation of Cx26 | Bicego, M; Beltramello, M; Melchionda, S; Carella, M; Piazza, V; Zelante, L; Bukauskas, FF; Arslan, E; Cama, E; Pantano, S; Bruzzone, R; D'Andrea, P; Mammano, F | 2006 | 119 |
| Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease | Bicego, M; Morassutto, S; Hernandez, VH; Morgutti, M; Mammano, F; D'Andrea, P; Bruzzone, R | 2006 | 110 |
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