Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndrome - Inserm - Institut national de la santé et de la recherche médicale Access content directly
Journal Articles Allergy Year : 2022

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

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Human genetics Innate immunity
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https://www.hal.inserm.fr/inserm-03775119

Submitted on : Monday, September 12, 2022-12:15:56 PM

Last modification on : Wednesday, May 17, 2023-9:05:09 AM

Long-term archiving on: Tuesday, December 13, 2022-6:42:07 PM

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inserm-03775119 , version 1 (12-09-2022)

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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, 2022, Online ahead of print. ⟨10.1111/all.15411⟩. ⟨inserm-03775119⟩

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