Publications by authors named "Stephanie Certain"

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Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Jérôme Feldmann, Isabelle Callebaut, Graça Raposo, Stéphanie Certain, Delphine Bacq

Cell· November 2003

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Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.
Jérôme Feldmann, Anne-Marie Prieur, Pierre Quartier, Patrick Berquin, Stephanie Certain

Am J Hum Genet· July 2002

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Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.
Jérôme Feldmann, Françoise Le Deist, Marie Ouachée-Chardin, Stéphanie Certain, Sarah Alexander

Br J Haematol· June 2002

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