Associated Papers
Tackling the diagnosis of HA20 in children: challenges of a highly variable clinical and genetic spectrum.
Anselmi F et al.
Rmd Open, 2026
Unidirectional association of clonal hematopoiesis with atherosclerosis development.
Díez-Díez M et al.
Nature Medicine, 2024
39215150 (PubMed )
Supplement: 41591_2024_3213_MOESM3_ESM.xlsx › Supplementary_Table_7
Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases.
Bagyinszky E et al.
International Journal of Molecular Sciences, 2024
Unraveling the genetics of transformed splenic marginal zone lymphoma.
Grau M et al.
Blood Advances, 2023
36995085 (PubMed )
Supplement: BLOODA_ADV-2022-009415-mmc1.xlsx › ST7
The First Case of an Infant with Familial A20 Haploinsufficiency in Korea.
Kim HY et al.
Journal of Korean Medical Science, 2020
Select a paper to view details