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