Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3.
Related Research units
Abstract
Mutations of UNC13D are causative for familial haemophagocytic lymphohistiocytosis type 3 (FHL3; OMIM 608898).
Bibliographical data
| Original language | English |
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| Article number | 5 |
| ISSN | 0022-2593 |
| Publication status | Published - 2011 |
| pubmed | 21248318 |
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