Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Hypocomplementemic Urticarial Vasculitis[original query] |
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DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signaling. Journal of clinical immunology 2022 6 42 (6): 1310-1320. Tusseau Maud, Lovšin Ema, Samaille Charlotte, Pescarmona Rémi, Mathieu Anne-Laure, Maggio Maria-Cristina, Selmanovi? Velma, Debeljak Marusa, Dachy Angelique, Novljan Gregor, Janin Alexandre, Januel Louis, Gibier Jean-Baptiste, Chopin Emilie, Rouvet Isabelle, Goncalves David, Fabien Nicole, Rice Gillian I, Lesca Gaétan, Labalme Audrey, Romagnani Paola, Walzer Thierry, Viel Sebastien, Perret Magali, Crow Yanick J, Av?in Tadej, Cimaz Rolando, Belot Alexand |
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