Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations

Blood

Volumn 114, Issue 9, 2009, Pages 1900-1903

  Dumont, Bénédicte ^a   Lasne, Dominique ^b,c   Rothschild, Chantal ^b   Bouabdelli, Maxime ^a   Ollivier, Véronique ^a   Oudin, Claire ^a   Ajzenberg, Nadine ^a   Grandchamp, Bernard ^a   Jandrot Perrus, Martine ^a  

^a BICHAT HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN; GLYCOPROTEIN VI; MESSENGER RNA; FC RECEPTOR; FIBRINOGEN RECEPTOR; PLATELET MEMBRANE GLYCOPROTEIN VI;

ALLELE; ARTICLE; CASE REPORT; CHILD; CODON; DNA SEQUENCE; FEMALE; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; PRIORITY JOURNAL; SCHOOL CHILD; THROMBOCYTE; THROMBOCYTE COUNT; CHEMISTRY; EXON; GENETICS; INTRON; METABOLISM; MUTATION; PHENOTYPE; THROMBOCYTE ACTIVATION;

ALLELES; BLOOD PLATELETS; CHILD; CODON; COLLAGEN; EXONS; FEMALE; HUMANS; INTRONS; MUTATION; PHENOTYPE; PLATELET ACTIVATION; PLATELET MEMBRANE GLYCOPROTEINS; RECEPTORS, FC; RNA, MESSENGER;

EID: 70349263950     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2009-03-213504     Document Type: Article

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