MIAN, Agrima et al. Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid. Autopsy and Case Reports, São Paulo, v. 9, n. 3, p. e2019101, 2019. DOI: 10.4322/acr.2019.101. Disponível em: https://revistas.usp.br/autopsy/article/view/161034.. Acesso em: 30 apr. 2024.