Abstract
In this issue of Blood, Chinn et al report genetic findings in a large cohort of children with hemophagocytic lymphohistiocytosis (HLH), indicating that many cases may be explained by mutations in genes other than those required for lymphocyte cytotoxicity.1
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CITATION STYLE
APA
Tesi, B., & Bryceson, Y. T. (2018, July 5). HLH: Genomics illuminates pathophysiological diversity. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2018-05-845818
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