Marcin M. Gorski, Anna Lecchi, Eti A. Femia, Silvia La Marca, Andrea Cairo, Emanuela Pappalardo, Luca A. Lotta, Andrea Artoni, Flora Peyvandi. Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects. haematol [Internet]. 2019Sep.30 [cited 2024Apr.26];104(10):2084-90. Available from: https://haematologica.org/article/view/9091