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.
随便看	pb-cadherin2 pbcak pbcat pbcb pbcba pbcc pbccb pbccc pbcch pbccha pbccm pbcd pbc d7 pbcda pbcdfa pbce pbcec pbcf pbcfi pbcfr pbcg pbcga pbcgc pbcgme pbch