C Petit

Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome.

P Coumel, P. Coumel, C. Petit, 1996, Journal of molecular and cellular cardiology.

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex

U. Wolfrum, P. Cossart, C. Petit, 2000, The EMBO journal.

Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals.

C. Petit, M. Leibovici, E. Verpy, 1999, Proceedings of the National Academy of Sciences of the United States of America.

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

C. Petit, A. El-Amraoui, J. Hardelin, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counseling.

C. Petit, F. Denoyelle, E. Garabédian, 2001, Archives of otolaryngology--head & neck surgery.