Defective dimerization of von Willebrand factor subunits due to a Cys → Arg mutation in type IID von Willebrand disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 93, Issue 8, 1996, Pages 3581-3586

  Schneppenheim, R ^a   Brassard, J ^b   Krey, S ^a   Budde, U ^c   Kunicki, T J ^b   Holmberg, L ^d   Ware, J ^b   Ruggeri, Z M ^b  

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c Allgemeines Krankenhaus Eilbek   (Germany)

^d LUND UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYSTEINE; VON WILLEBRAND FACTOR;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; AUTOGRAPHA CALIFORNICA; BLEEDING TIME; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CONTROLLED STUDY; DIMERIZATION; DISULFIDE BOND; DNA SEQUENCE; FEMALE; HUMAN; NONHUMAN; PRIORITY JOURNAL; VON WILLEBRAND DISEASE;

ANIMALS; BACULOVIRIDAE; BASE SEQUENCE; CELL LINE; DISULFIDES; DNA; DNA PRIMERS; FEMALE; GENE EXPRESSION; HETEROZYGOTE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MOLECULAR WEIGHT; PEDIGREE; POINT MUTATION; PROTEIN CONFORMATION; RECOMBINANT PROTEINS; SPODOPTERA; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 0029916821     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.8.3581     Document Type: Article

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