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Article

Hodgkin lymphoma in an individual with TREX1-mediated Aicardi Goutières syndrome.

Pediatric blood & cancer - 1 Jan 2022

Gavazzi Francesco, Fraser Jamie L, Bloom Miriam, Tochen Laura, Rhee Jullie, Kwan Megan, Victoria Teresa, Teachey David T, Ho Cheng-Ying, Vanderver Adeline, Linn Rebecca L

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Share to Autoimmune Diseases of the Nervous System
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 34490982
DOI: 10.1002/pbc.29322
PMCID: PMC11348674

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hodgkin lymphoma in an individual with TREX1-mediated Aicardi Goutières syndrome.PMID 34490982Read ↗

Clinical heterogeneity among a three-generation Japanese family with D18N TREX1 mutation for Aicardi-Goutières syndrome / familial chilblain lupusSemantic proximity Read ↗

Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus.Semantic proximity Read ↗

Systemic involvement in TREX1-associated familial chilblain lupus.Semantic proximity Read ↗

Aicardi-Goutières Syndrome Is Caused by IFIH1 MutationsSemantic proximity Read ↗

Phenotypic and Molecular Spectrum of Aicardi-Goutières Syndrome: A Study of 24 PatientsSemantic proximity Read ↗

Human disease phenotypes associated with mutations in TREX1.Semantic proximity Read ↗

Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome.Semantic proximity Read ↗

A case of Aicardi-Goutières syndrome caused by TREX1 gene mutation.Semantic proximity Read ↗

Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.Semantic proximity Read ↗

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune responseSemantic proximity Read ↗

Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family membersSemantic proximity Read ↗

SAMHD1 Mutations Are Also Responsible for Aicardi-Goutières in the Cree Population.Semantic proximity Read ↗

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