Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid

Por Agrima Mian, Kalpana Kumari, Seema Kaushal, Farhan Fazal, Parul Kodan, Atul Batra, Prabhat Kumar, Upendra Baitha, Pankaj Jorwal, Manish Soneja, Mehar Chand Sharma, Ashutosh Biswas
Publicado no Autopsy and Case Reports (2019)