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Article

Novel somatic mutations in UBA1 as a cause of VEXAS syndrome.

Blood - 1 Jul 2021

Poulter James A, Collins Jason C, Cargo Catherine, De Tute Ruth M, Evans Paul, Ospina Cardona Daniela, Bowen David T, Cunnington Joanna R, Baguley Elaine, Quinn Mark, Green Michael, McGonagle Dennis, Beck David B, Werner Achim, Savic Sinisa

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Share to Autoimmune and Inflammatory Disorders Research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33690815
DOI: 10.1182/blood.2020010286
PMCID: PMC8462400

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Related research

Semantic proximity does not establish scientific evidence.

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Novel somatic mutations in UBA1 as a cause of VEXAS syndrome.PMID 33690815Read ↗

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Novel Somatic UBA1 Variant in a Patient With VEXAS Syndrome.Semantic proximity Read ↗

Somatic mutations cause VEXAS syndrome.Semantic proximity Read ↗

An update on VEXAS syndrome.Semantic proximity Read ↗

Atypical splice-site mutations causing VEXAS syndrome.Semantic proximity Read ↗

UBA1 dysfunction in VEXAS and cancer.Semantic proximity Read ↗

Behçet's disease with a somatic UBA1 variant:Expanding spectrum of autoinflammatory phenotypes of VEXAS syndromeSemantic proximity Read ↗

Somatic mutations in VEXAS Syndrome and Erdheim-Chester disease: Inflammatory myeloid diseases.Semantic proximity Read ↗

Description of a novel splice site variant in UBA1 gene causing VEXAS syndrome.Semantic proximity Read ↗

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