https://doi.org/10.4322/acr.2019.101
Autops Case Rep, vol.9, e2019101 Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid Epstein–Barr Virus Nuclear Antigens, Familial Hemophagocytic Lymphohistiocytosis, Lymphoma, Perforin Gene Mutation Article / Autopsy Case Report
Autops Case Rep, vol.9, e2019101 Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid Epstein–Barr Virus Nuclear Antigens, Familial Hemophagocytic Lymphohistiocytosis, Lymphoma, Perforin Gene Mutation Article / Autopsy Case Report