Publications by authors named "Stephanie Audebert"

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Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.
Fabienne Lesueur, Bakar Bouadjar, Caroline Lefèvre, Florence Jobard, Stéphanie Audebert

J Invest Dermatol· April 2007

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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
Caroline Lefévre, Stéphanie Audebert, Florence Jobard, Bakar Bouadjar, Hakima Lakhdar

Hum Mol Genet· September 2003

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Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.
Slaheddine Marrakchi, Stéphanie Audebert, Bakar Bouadjar, Christina Has, Caroline Lefèvre

J Invest Dermatol· March 2003

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