Scott syndrome

recessively inherited coagulation disorder due to defective or absent scramblase (protein that is necessary to take a coagulation enzyme from inside the cell membrane to outside to signal the beginning of coagulation).

Scott syndrome

A mild bleeding disorder (OMIM:262890) caused by impaired surface exposure of procoagulant phosphatidylserine on platelets and other circulating cells after activation with Ca2+-elevating agents.
Molecular pathology
ANO5 mutations cause Scott syndrome.

单词	scott syndrome
释义	Scott syndrome Scott syndrome recessively inherited coagulation disorder due to defective or absent scramblase (protein that is necessary to take a coagulation enzyme from inside the cell membrane to outside to signal the beginning of coagulation). Scott syndrome recessively inherited coagulation disorder due to defective or absent scramblase (protein that is necessary to take a coagulation enzyme from inside the cell membrane to outside to signal the beginning of coagulation). Scott syndrome A mild bleeding disorder (OMIM:262890) caused by impaired surface exposure of procoagulant phosphatidylserine on platelets and other circulating cells after activation with Ca2+-elevating agents. Molecular pathology ANO5 mutations cause Scott syndrome.
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