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Volumn 60, Issue 4, 1999, Pages 309-310
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Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand disease
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Author keywords
Type 2A vWD; Von Willebrand disease; Von Willebrand factor
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Indexed keywords
ARGININE;
GLYCINE;
ALLELISM;
AMINO ACID SUBSTITUTION;
ARTICLE;
GENE MUTATION;
HUMAN;
MISSENSE MUTATION;
PHASE TRANSITION;
PRIORITY JOURNAL;
THROMBOCYTE FUNCTION;
VON WILLEBRAND DISEASE;
ARGININE;
BASE SEQUENCE;
DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC;
FEMALE;
GLYCINE;
HUMANS;
MALE;
MUTATION;
PEDIGREE;
SPAIN;
VON WILLEBRAND DISEASE;
VON WILLEBRAND FACTOR;
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EID: 0345003925
PISSN: 03618609
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1096-8652(199904)60:4<309::AID-AJH10>3.3.CO;2-G Document Type: Article |
Times cited : (6)
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References (7)
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