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

Mian, Agrima; Kumar, Kalpana; Kaushal, Seema; Fazal, Farhan; Kodan, Parul; Batra, Atul; Kumar, Prabhat; Baitha, Upendra; Jorwal, Pankaj; Soneja, Manish; Sharma, Mehar Chand; Biswas, Ashutosh

Autopsy and Case Reports; Vol. 9 Núm. 3 (2019); e2019101

Universidade de São Paulo. Hospital Universitário 2019-08-14

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Deste Autor:

  1. Kaushal, S
  2. Kumar, P
  3. Fazal, F
  4. Biswas, A
  5. Jorwal, P

Neste Assunto:

  1. Lymphoma
  2. Barr Virus Nuclear Antigens
  3. Epstein
  4. Perforin Gene Mutation
  5. Familial Hemophagocytic Lymphohistiocytosis

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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