Christine Petit

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.

J. Sahel, S. Picaud, C. Petit, 1996, Human molecular genetics.

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

C. Petit, D. Weil, A. Adato, 1997, American journal of human genetics.