Molecular characterization of two mutations in platelet glycoprotein (GP) Ibα in two Finnish Bernard-Soulier syndrome families

European Journal of Haematology

Volumn 62, Issue 3, 1999, Pages 160-168

  Koskela, S ^a   Partanen, J ^a   Salmi, T T ^b   Kekomaki R ^a  

^a FINNISH RED CROSS BLOOD SERVICE   (Finland)

^b TURKU UNIVERSITY HOSPITAL   (Finland)

Author keywords

Bernard; Finnish disease heritage; Glycoprotein Ib IX V; Platelet; Soulier syndrome

Indexed keywords

GLYCOPROTEIN IB;

ARTICLE; BERNARD SOULIER DISEASE; BLEEDING TIME; CASE REPORT; FEMALE; FINLAND; FLOW CYTOMETRY; GENE MUTATION; HUMAN; INFANT; MOLECULAR GENETICS; MULTIGENE FAMILY; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SUBENDOTHELIUM; THROMBOCYTE AGGREGATION; THROMBOCYTOPENIA;

EID: 0033026126     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0609.1999.tb01739.x     Document Type: Article

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