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Clinical Features - Original Research

MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience

ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon show all
Pages 68-72 | Received 10 Sep 2018, Accepted 22 Nov 2018, Published online: 12 Dec 2018

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