factor v g1691a造句

• Overall, " factor V G1691A " mutation has been linked to the development of porencephaly.
• The results indicated that there was higher prevalence of the " factor V G1691A " mutation in the porencephalic patient group.
• Another genetic mutation, " factor V G1691A " mutation, has been reported to show possible association to the development of porencephaly.
• A mutation in " factor V G1691A " increases the risk of thrombosis, blood clots, in neonates, infants, and children.
• Therefore, 76 porencephalic and 76 healthy infants were investigated for " factor V G1691A " mutation along with other different prothrombotic risk factors.
• The prediction that childhood porencephaly is caused by hypercoagulable state, a condition where one has a higher chance of developing blood clots, was supported by the significance of the " factor V G1691A " mutation.