Abstract

In this issue of Blood, Stevenson et al describe a family with a homozygous missense mutation in FLI1 that is associated with a platelet phenotype identical to the one observed in Paris-Trousseau syndrome, supporting existing evidence that FLI1 is directly involved in the mechanism of thrombocytopenia observed in this disease.1.

Original languageEnglish
Pages (from-to)1973-1974
Number of pages2
JournalBlood
Volume126
Issue number17
DOIs
StatePublished - Oct 22 2015

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