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Volumn 96, Issue 7, 2000, Pages 2501-2505

A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; FIBRINOGEN; MESSENGER RNA; PROTEIN SUBUNIT;

EID: 0034307690     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v96.7.2501     Document Type: Article
Times cited : (37)

References (28)
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  • 7
    • 0002028933 scopus 로고
    • Nucleotide sequences of the three genes coding for human fibrinogen
    • Liu CY, Chien S, eds. Fibrinogen, Thrombosis, Coagulation and Fibrinolysis. New York, NY: Plenum
    • (1990) , pp. 39-48
    • Chung, D.W.1    Harris, J.E.2    Davie, E.W.3
  • 13
    • 0023683667 scopus 로고
    • How eukaryotic transcriptional activators work
    • (1988) Nature , vol.335 , pp. 683-689
    • Ptashne, M.1
  • 15
    • 0034651759 scopus 로고    scopus 로고
    • Missense mutations in the human β fibrinogen gene causes congenital afibrinogenemia by impairing fibrinogen secretion
    • (2000) Blood , vol.95 , pp. 1336-1341
    • Duga, S.1    Asselta, R.2    Santagostino, E.3
  • 20
    • 0025119635 scopus 로고
    • Fibrinogen as a major risk factor in cardiovascular disease
    • (1990) TIPS , vol.11 , pp. 444-451
    • Cook, N.S.1    Ubben, D.2
  • 26
    • 0023216744 scopus 로고
    • A new mutation in IVS-1 of the human β-globin gene causing β thalassemia due to abnormal splicing
    • (1987) Blood , vol.70 , pp. 147-151
    • Atweh, G.F.1    Wong, C.2    Reed, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.