TY - CHAP
T1 - The Molecular Basis of Von Willebrand Disease
AU - Baronciani, Luciano
AU - Mannucci, Pier Mannuccio
PY - 2010/3/10
Y1 - 2010/3/10
KW - Gene encoding VWF-mapped on chromosome 12
KW - Molecular basis of von Willebrand disease
KW - Transfusional therapy with plasma products containing FVIII and VWF-treatment of choice
KW - Type 2 VWD-approximately 20% of all VWD cases
KW - Type 3 VWD, autosomal recessive severe disorder-and nearly complete absence of VWF
KW - Von Willebrand disease (VWD)-common inherited bleeding disorder
KW - Von Willebrand disease and its classification
KW - Von Willebrand factor in primary hemostasis
KW - VWD and deficiency or multimeric plasma glycoprotein dysfunction of von Willebrand factor (VWF)
KW - VWF multimer synthesis and subcellular localization of post-translational modification events
UR - http://www.scopus.com/inward/record.url?scp=84874387251&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84874387251&partnerID=8YFLogxK
U2 - 10.1002/9781444318531.ch19
DO - 10.1002/9781444318531.ch19
M3 - Chapter
AN - SCOPUS:84874387251
SN - 9781405182317
SP - 233
EP - 245
BT - Molecular Hematology: Third Edition
PB - Wiley-Blackwell
ER -