C. Petit

Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness

D. Weil, J. Perea, R. Bruzzone, 2001, Cell communication & adhesion.

Loss‐of‐function and residual channel activity of connexin26 mutations associated with non‐syndromic deafness

S. Marlin, R. Bruzzone, C. Petit, 2003, FEBS letters.