INFEVERS: The Registry for FMF and hereditary inflammatory disorders mutations

Sarrauste De Menthière N., Terrière Stéphane, Pugnère Denis, Ruiz Manuel, Demaille Jacques, Touitou Isabelle. 2003. INFEVERS: The Registry for FMF and hereditary inflammatory disorders mutations. Nucleic Acids Research, 31 (1) : pp. 282-285.

Journal article ; Article de revue à facteur d'impact
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Abstract : We have established the INFEVERS - INternet periodic FEVERS - website (which is freely accessible at Our objectives were to develop a specialist site to gather updated information on mutations responsible for hereditary inflammatory disorders: i.e. Familial Mediterranean Fever (FMF), TRAPS (TNF Receptor 1A Associated Syndrome), HIDS (HyperIgD Syndrome), MWS (Muckle-Wells Syndrome)/FCU (Familial Cold Urticaria)/CINCA (Chronic Infantile Neurological Cutaneous and Articular Syndrome). Contributors submit their novel mutations through a 3 step form. Depending on the disease concerned, a member of the editorial board is automatically solicited to overview and validate new submissions, via a special secured web interface. If accepted, the new mutation is available on the INFEVERS web site and the discoverer, who is informed by email, is credited by having his/her name and date of the discovery on the site. The INFEVERS gateway provides researchers and clinicians with a common access location for information on similar diseases, allowing a rapid overview of the corresponding genetic defects at a glance. Furthermore, it is interactive and extendable according to the latest genes discovered. (Résumé d'auteur)

Classification Agris : C30 - Documentation and information
F30 - Plant genetics and breeding

Auteurs et affiliations

  • Sarrauste De Menthière N., IGH (FRA)
  • Terrière Stéphane, IGH (FRA)
  • Pugnère Denis, IGH (FRA)
  • Ruiz Manuel, CIRAD-CP-PALMIER (FRA) ORCID: 0000-0001-8153-276X
  • Demaille Jacques, IGH (FRA)
  • Touitou Isabelle, Centre hospitalier universitaire Arnaud-de-Villeneuve (FRA)

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