Novel mutation in bernard-soulier syndrome

Transfusion Medicine and Hemotherapy

Volumn 37, Issue 5, 2010, Pages 278-283

  Sandrock, Kirstin ^a   Knöfler, Ralf ^b   Greinacher, Andreas ^c   Fürll, Birgitt ^c   Gerisch, Sebastian ^a   Schuler, Ulrich ^d   Gehrisch, Siegmund ^d   Busse, Anja ^a   Zieger, Barbara ^a,e  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY HOSPITAL CARL GUSTAV CARUS   (Germany)

^c UNIVERSITY OF GREIFSWALD   (Germany)

^d DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^e UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Bernard Soulier syndrome; Bleeding complications; Flow cytometry; Genetic abnormalities; Novel deletion; Platelet glycoprotein Ib IX; Thrombocytopenia

Indexed keywords

GLYCOPROTEIN IB; VON WILLEBRAND FACTOR;

ADULT; ARTICLE; BERNARD SOULIER DISEASE; BLEEDING; CASE REPORT; FLOW CYTOMETRY; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; IMMUNOFLUORESCENCE; MALE; PHENOTYPE; SEQUENCE ANALYSIS; THROMBOCYTE FUNCTION; THROMBOCYTOPENIA;

EID: 77957837264     PISSN: 16603796     EISSN: None     Source Type: Journal    
DOI: 10.1159/000320255     Document Type: Article

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