Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection

L. Alsina, R. Colobran, M. F. De Sevilla, A. Català, L. Viñas, S. Ricart, A. M. Plaza, S. Lois, M. Juan, R. Pujol-Borrell, M. Martinez-Gallo

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