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. The gene discussed is GP6; the disease is hyperinsulinemic hypoglycemia, familial, 4.