Moreover, the hemorrhagic manifestations in patients with GPVI deficiency are generally milder compared to those observed in individuals with Glanzmann’s thrombasthenia or Bernard-Soulier Syndrome, suggesting that GPVI plays a less critical role in hemostasis than GPIIbIIIa or the GPIb-IX-V complex. Here, GP6 is linked to Glanzmann thrombasthenia 1.