Which is the most common FVIII mutation in patients with a severe phenotype (occurring in almost 50% of patients) ?
A) Gross deletion of entire gene locus
B) Point mutation involving the thrombin cleavage site
C) Inversion mutation of intron 22
D) Point mutation involving the site of VWF attachment
Correct Answer:
Verified
Q18: A physician has confirmed von Willebrand's disease
Q19: A 34-year-old woman has just given birth
Q20: Which of the following is used in
Q21: Deficiencies of the fibrin-forming proteins often have
Q22: What plasma factor levels of the deficient
Q24: Which of the following laboratory assays would
Q25: How does von Willebrand's disease (VWD) differ
Q26: Explain why disseminated intravascular coagulation is not
Q27: Explain the inheritance pattern of the following
Q28: Explain how liver disease can be differentiated
Unlock this Answer For Free Now!
View this answer and more for free by performing one of the following actions
Scan the QR code to install the App and get 2 free unlocks
Unlock quizzes for free by uploading documents