Article

Turkish DIRA patient with novel IL1RN gene mutation

2015-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 4bd3f3de-72b2-5b2b-9a7f-b87d50e5e3a0
DOI: 10.1186/1546-0096-13-s1-p181
PMCID: PMC4599864

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Turkish DIRA patient with novel IL1RN gene mutationDOI 10.1186/1546-0096-13-s1-p181Read

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

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

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

Case report: Novel compound heterozygous IL1RN mutations as the likely cause of a lethal form of deficiency of interleukin-1 receptor antagonist.Semantic proximity Read

Novel mutation of the LPIN2 gene in Turkish brothers with Majeed syndrome. Response to IL-1 inhibitionSemantic proximity Read

P02-002 - IL36RN mutations in patients with DITRASemantic 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

A novel mutation of IL1RN in the deficiency of interleukin-1 receptor antagonist syndrome: description of two unrelated cases from Brazil.Semantic proximity Read

Novel heterozygous mutation of RTEL1 in interstitial pneumonia with autoimmune feature.Semantic proximity Read

Compound Heterozygous Mutations of IL12RB1 in a Patient with Selective Defects in Th17 Differentiation.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

IRF2BPL gene variants: One new case.Semantic proximity Read