The Functional Basis for Hemophagocytic Lymphohistiocytosis in a Patient with Co-inherited Missense Mutations in the Perforin (PFN1) Gene
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J. Trapani | S. Jane | I. Voskoboinik | M. Smyth | P. Darcy | E. Cretney | K. Browne | J. Jackson | Marie-Claude Thia | A. D. de Bono