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 language | English |
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Pages (from-to) | 1973-1974 |
Number of pages | 2 |
Journal | Blood |
Volume | 126 |
Issue number | 17 |
DOIs | |
State | Published - Oct 22 2015 |