Hodgkin lymphoma in an individual with TREX1 ‐mediated Aicardi Goutières syndrome-Reference-Cited by-同舟云学术

Hodgkin lymphoma in an individual with TREX1 ‐mediated Aicardi Goutières syndrome

Published:2021-09-07 Issue:1 Volume:69 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Gavazzi Francesco¹²^ORCID,Fraser Jamie L.³,Bloom Miriam⁴,Tochen Laura⁵,Rhee Jullie⁵,Kwan Megan¹,Victoria Teresa⁶,Teachey David T.⁷⁸,Ho Cheng‐Ying⁹,Vanderver Adeline¹¹⁰,Linn Rebecca L.¹¹

Affiliation:

1. Division of Neurology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Department of Molecular and Translational Medicine University of Brescia Brescia Italy

3. Rare Disease Institute, Division of Genetics and Metabolism Children's National Hospital Washington District of Columbia USA

4. Department of Pediatrics Children's National Hospital Washington District of Columbia USA

5. Department of Neurology Children's National Hospital Washington District of Columbia USA

6. Division of Radiology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

7. Divisions of Hematology and Oncology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

8. Divisions of Hematology and Oncology University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA

9. Department of Pathology and Neurology University of Maryland School of Medicine Baltimore Maryland USA

10. Department of Neurology, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

11. Department of Pathology and Lab Medicine at Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29322

Reference13 articles.

1. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

2. Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

3. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

4. History of autoimmune conditions and lymphoma prognosis

5. Hodgkin lymphoma: A review and update on recent progress

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