TY  - GEN
AU  - Mancuso,D J
AU  - Kroner,P A
AU  - Christopherson,P A
AU  - Vokac,E A
AU  - Gill,J C
AU  - Montgomery,R R
TI  - Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets
SN  - 0006-4971
PY  - 1996///1107
KW  - Alleles
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Blood Platelets
KW  - metabolism
KW  - Crotalid Venoms
KW  - pharmacology
KW  - DNA Mutational Analysis
KW  - Female
KW  - Heparin
KW  - Heterozygote
KW  - Humans
KW  - Male
KW  - Molecular Sequence Data
KW  - Pedigree
KW  - Phenotype
KW  - Platelet Membrane Glycoproteins
KW  - Protein Binding
KW  - drug effects
KW  - Protein Structure, Tertiary
KW  - Receptors, Cell Surface
KW  - Recombinant Fusion Proteins
KW  - Ristocetin
KW  - Sequence Alignment
KW  - Sequence Deletion
KW  - Sequence Homology
KW  - von Willebrand Diseases
KW  - classification
KW  - von Willebrand Factor
KW  - chemistry
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
ER  -