Ahmed A, Montague SJ, Vyas H, Mistry J, Pavey NJ, Smith SR, Griffith L, Clothier I, Hudson R, Faulkner E, Buka R, Bignell P, Fratter C, Marshall K, Bailiff B, Poulter NS, de Laat B, Huskens D, Lowe GC, Thomas SG, Morgan NV. Scott syndrome with novel compound heterozygous pathogenic variants in <i>ANO6</i&gt; and reduced thrombin generation. Haematologica; https://doi.org/10.3324/haematol.2025.300111 [Early view].