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Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndrome

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https://www.hal.inserm.fr/inserm-03775119
Contributor : Sandrine Couvet Connect in order to contact the contributor
Submitted on : Monday, September 12, 2022 - 12:15:56 PM
Last modification on : Wednesday, September 14, 2022 - 4:03:48 AM

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Allergy_2022_15411.pdf
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Camille Louvrier, Fawaz Awad, Serge Amselem, Dan Lipsker, Irina Giurgea. Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndrome. Allergy, Wiley, 2022, Online ahead of print. ⟨10.1111/all.15411⟩. ⟨inserm-03775119⟩

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