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- W4220794852 abstract "Patients with primary hemophagocytic lymphohistiocytosis may present with different mutations and phenotypic findings. It is usually presented as case reports because of its rare occurrence. Here, we discuss a case diagnosed with familial hemophagocytic lymphohistiocytosis 3, that presented in the neonatal period and was detected to have homozygous UNC13D and heterozygous STX11 mutations." @default.
- W4220794852 created "2022-04-03" @default.
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- W4220794852 date "2022-03-16" @default.
- W4220794852 modified "2023-10-14" @default.
- W4220794852 title "Familial Hemophagocytic Lymphohistiocytosis With Heterozygous STX11 and Homozygous UNC13D Mutations Diagnosed in the Neonatal Period" @default.
- W4220794852 doi "https://doi.org/10.1097/mph.0000000000002449" @default.
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- W4220794852 hasPublicationYear "2022" @default.
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