Bernard-Soulier syndrome: Common ancestry in two African American families with the GP Ibα Leu129Pro mutation

American Journal of Hematology

Volumn 65, Issue 2, 2000, Pages 141-148

  Antonucci, John Vito ^a   Martin, Eric S ^a   Hulick, Peter J ^a   Joseph, Abraham ^a   Eric Martin, S ^a  

^a CHRISTIANA CARE HEALTH SYSTEM   (United States)

Author keywords

African American families; Bernard Soulier syndrome; GP Ib mutation

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BERNARD SOULIER DISEASE; BLEEDING DISORDER; BLEEDING TIME; CHROMOSOMAL LOCALIZATION; CHROMOSOME 17P; DISULFIDE BOND; ETHNIC GROUP; GENE MUTATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; RACE DIFFERENCE; THROMBOCYTE FUNCTION;

AFRICA; AFRICAN CONTINENTAL ANCESTRY GROUP; BERNARD-SOULIER SYNDROME; CHROMOSOMES, HUMAN, PAIR 17; CONSENSUS SEQUENCE; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HOMOZYGOTE; HUMANS; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX; POINT MUTATION; POLYMORPHISM, GENETIC; UNITED STATES;

EID: 0033828392     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8652(200010)65:2<141::AID-AJH9>3.0.CO;2-H     Document Type: Article

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