The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene (Q36399692)
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English | The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene |
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The functional basis for hemophagocytic lymphohistiocytosis in a patient with co-inherited missense mutations in the perforin (PFN1) gene (English)
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Jacob T Jackson
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Erika Cretney
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Ilia Voskoboinik
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Marie-Claude Thia
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Annette De Bono
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Kylie Browne
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14 September 2004
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811-816
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