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Volumn 145, Issue 3, 2009, Pages 433-435

Double mutations causing haemophilia B: A double whammy!

Author keywords

Conformation sensitive gel electrophoresis; Double mutations; Haemophilia B

Indexed keywords

BLOOD CLOTTING FACTOR 9;

EID: 64149087231     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2009.07618.x     Document Type: Article
Times cited : (10)

References (8)
  • 2
    • 64149091032 scopus 로고    scopus 로고
    • Mutation detection in promoter region of coagulation factor IX in haemophilia B patients in Iran
    • Abstract 1465.
    • Farsani, M.A., Rastegar, G., Kazemi, A., Ala, F., Mohammadi, M., Ravanbood, S. Allahbakhshian, A. (2008) Mutation detection in promoter region of coagulation factor IX in haemophilia B patients in Iran. Haematologica, 93 (Suppl. 1 553. Abstract 1465.
    • (2008) Haematologica , vol.93 , Issue.SUPPL. 1 , pp. 553
    • Farsani, M.A.1    Rastegar, G.2    Kazemi, A.3    Ala, F.4    Mohammadi, M.5    Ravanbood, S.6    Allahbakhshian, A.7
  • 6
    • 33947608488 scopus 로고    scopus 로고
    • A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population
    • Quadros, L., Ghosh, K. Shetty, S. (2007) A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population. Annals of Hematology, 86, 377 379.
    • (2007) Annals of Hematology , vol.86 , pp. 377-379
    • Quadros, L.1    Ghosh, K.2    Shetty, S.3
  • 7
    • 0027244515 scopus 로고
    • Molecular biology of hemophilia B
    • Roberts, H.R. (1993) Molecular biology of hemophilia B. Thrombosis and Haemostasis, 70, 1 9.
    • (1993) Thrombosis and Haemostasis , vol.70 , pp. 1-9
    • Roberts, H.R.1
  • 8
    • 0031957807 scopus 로고    scopus 로고
    • Precise carrier and prenatal diagnosis in families with hemophilia A. Use of conformation sensitive gel electrophoresis for rapid mutation screening and polymorphism analysis
    • Williams, I.J., Abuzendah, A., Winship, P.R., Preston, F.E., Dolan, G., Wright, J., Peake, I.R. Goodeve, A.C. (1998) Precise carrier and prenatal diagnosis in families with hemophilia A. Use of conformation sensitive gel electrophoresis for rapid mutation screening and polymorphism analysis. Thrombosis and Haemostasis, 79, 723 726.
    • (1998) Thrombosis and Haemostasis , vol.79 , pp. 723-726
    • Williams, I.J.1    Abuzendah, A.2    Winship, P.R.3    Preston, F.E.4    Dolan, G.5    Wright, J.6    Peake, I.R.7    Goodeve, A.C.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.