Associated Papers
Prevalence and impact of molecular variation in the three-prime repair exonuclease 1 TREX1 and its implications for oncology.
Shekfeh M et al.
Human Genomics, 2025
40581636 (PubMed )
Supplement: 40246_2025_785_MOESM11_ESM.xlsx › Table_S8
How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study.
Tan RYY et al.
Neurology, 2019
Rare variants of the 3'-5' DNA exonuclease TREX1 in early onset small vessel stroke.
McGlasson S et al.
Wellcome Open Research, 2017
Human disease phenotypes associated with mutations in TREX1.
Rice GI et al.
Journal of Clinical Immunology, 2015
Select a paper to view details