Glanzmann thrombasthenia associated with a 21-amino acid deletion (Leu817-Gln837) in glycoprotein IIb due to abnormal splicing in exon 25

International Journal of Hematology

Volumn 80, Issue 1, 2004, Pages 83-90

  Fujimoto, Tetsuro Takahiro ^a,b   Sora, Mihoko ^a   Ide, Kazuko ^a   Mizushima, Miyoko ^a   Mita, Masashi ^a   Nishimura, Shinichiro ^b   Ueda, Kazuhiro ^b   Fujimura, Kingo ^a  

^a Program for Applied Biomedicine   (Japan)

^b HIROSHIMA UNIVERSITY   (Japan)

Author keywords

Calf 2 domain; Glanzmann thrombasthenia; GPIIb IIIa complex; Intracellular transport; Platelets

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; FIBRINOGEN RECEPTOR; GLYCOPROTEIN IIB; MESSENGER RNA;

AMINO ACID SEQUENCE; ARTICLE; BASE PAIRING; BINDING SITE; CALF 2 DOMAIN; CASE REPORT; CELL LYSATE; COMPLEX FORMATION; EXON; FEMALE; GENE DELETION; GENETIC DISORDER; GLANZMANN DISEASE; HUMAN; IMMUNOHISTOCHEMISTRY; IMMUNOPRECIPITATION; INTRACELLULAR TRANSPORT; PRESCHOOL CHILD; PROTEIN DOMAIN; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; RNA SPLICING;

ANTIGENS, SURFACE; BLOTTING, WESTERN; EXONS; FEMALE; FLOW CYTOMETRY; GENE DELETION; HUMANS; INFANT; PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX; PLATELET MEMBRANE GLYCOPROTEIN IIB; RNA SPLICING; THROMBASTHENIA;

EID: 3142769772     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1532/IJH97.04001     Document Type: Article

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