,

Radha Ramanan1, Andreas Verstraete2, Christine Van Laer3

  • 1Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium; Australian Centre for Blood Diseases, Monash University, Melbourne, Victoria, Australia; Department of Human Molecular Pathology, Alfred Hospital, Melbourne, Victoria, Australia.

概括

多基因面板通过同时评估多个基因来增强出血,血小板和血栓性疾病 (BPTD) 的诊断. 在临床实施,变异解释和遗传测试的伦理考虑方面仍然存在挑战.