Friend leukemia integration 1 transcription factor

[1]. Jacqueline Stockley, et al. Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects. Blood. 2013 Dec 12;122(25):4090-3. [Content Brief]

[2]. Paul Saultier, et al. Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features. Haematologica. 2017 Jun;102(6):1006-1016. [Content Brief]

[3]. William S Stevenson, et al. Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1. Blood. 2015 Oct 22;126(17):2027-30. [Content Brief]