Associated Papers
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variants.
Wegehaupt O et al.
Blood, 2025
40090000 (PubMed )
Supplement: BLOOD_BLD-2024-027954-mmc2.xlsx › Suppl._table_1
Characterization of immune cells and perforin mutations in familiar venous thromboembolism.
Duan Q et al.
International Journal of Clinical and Experimental Medicine, 2015
Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.
An O et al.
Protein Science : a Publication of the Protein Society, 2013
Variations of the perforin gene in patients with multiple sclerosis.
Cappellano G et al.
Genes and Immunity, 2008
Select a paper to view details