Bernard-Soulier syndrome with severe bleeding: Absent platelet glycoprotein Ib alpha due to a hamozygous one-base deletion

Thrombosis and Haemostasis

Volumn 76, Issue 5, 1996, Pages 670-674

  Li, Chaoyang ^b   Pasquale, Dominick N ^a   Roth, Gerald J ^b,c  

^a S Francis Hosp and Medical Center   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE RECEPTOR; GLYCOPROTEIN IB; MEMBRANE PROTEIN; VON WILLEBRAND FACTOR;

ADULT; ALLELE; ARTICLE; BERNARD SOULIER DISEASE; BLEEDING; CASE REPORT; CODON; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GASTROINTESTINAL HEMORRHAGE; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; HYBRIDIZATION; LIGAND BINDING; MALE; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DEFICIENCY; SOUTHERN BLOTTING; THROMBOCYTE; THROMBOCYTE AGGREGATION; THROMBOCYTOPENIA;

EID: 0029910888     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0038-1650640     Document Type: Article

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