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pubmed-article:21248318pubmed:abstractTextMutations of UNC13D are causative for familial haemophagocytic lymphohistiocytosis type 3 (FHL3; OMIM 608898).lld:pubmed
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pubmed-article:21248318pubmed:articleTitleGenotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3.lld:pubmed
pubmed-article:21248318pubmed:affiliationDepartment of Pediatric Hematology and Oncology, Azienda Ospedaliero-Universitaria Meyer, Florence, Italy.lld:pubmed
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