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Article

Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA).

Journal of clinical immunology - 1 May 2020

Ziaee Vahid, Youssefian Leila, Faghankhani Masoomeh, Jazayeri Ali, Saeidian Amir Hossein, Vahidnezhad Hassan, Uitto Jouni

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32170523
DOI: 10.1007/s10875-020-00767-w

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Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA).PMID 32170523Read ↗

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A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatmentSemantic proximity Read ↗

Deficiency of Interleukin-1 Receptor Antagonist Due to Novel IL1RN Pathogenic Variants: A 40 Year-Long Journey Until Its DiagnosisSemantic proximity Read ↗

A case report of a novel compound heterozygous mutation in a Brazilian patient with deficiency of Interleukin-1 receptor antagonist (DIRA).Semantic proximity Read ↗

Deficiency of Interleukin-1 Receptor Antagonist (DIRA): Report of the First Indian Patient and a Novel Deletion Affecting IL1RN.Semantic proximity Read ↗

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Analysis of Anakinra therapy for the Deficiency of Interleukin-1 Receptor Antagonist through Clinical EvidenceSemantic proximity Read ↗

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