Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(Δ597-1008) to form stable complexes with GPIIIa

Thrombosis and Haemostasis

Volumn 87, Issue 4, 2002, Pages 684-691

  Arias Salgado, Elena G ^a   Tao, Jianming ^a   González Manchón, Consuelo ^a   Butta, Nora ^a   Vicente, Vicente ^a   Ayuso, Matilde S ^a   Parrilla, Roberto ^a  

^a CENTRO DE INVESTIGACIONES BIOLÓGICAS   (Spain)

Author keywords

Fibrinogen receptor; Glanzmann's thrombasthenia; GPIIb; GPIIIa; Green fluorescence protein

Indexed keywords

BETA ACTIN; DNA; FIBRINOGEN RECEPTOR; GLYCOPROTEIN IIB; GLYCOPROTEIN IIIA; MESSENGER RNA;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; BLEEDING TIME; CASE REPORT; CELL SURFACE; CHO CELL; COMPLEX FORMATION; DISEASE CLASSIFICATION; DNA POLYMORPHISM; DNA SEQUENCE; EXON; FLOW CYTOMETRY; GENETIC ANALYSIS; GENETIC STABILITY; GENOTYPE PHENOTYPE CORRELATION; GLANZMANN DISEASE; HOMOZYGOSITY; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; MALE; NONHUMAN; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCHOOL CHILD; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON; THROMBOCYTE;

EID: 0036212986     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1613066     Document Type: Article

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