Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi Jews.

Berg, L P; Varon, D; Martinowitz, U; Wieland, K; Kakkar, V V; Cooper, D N

Berg, L P; Varon, D; Martinowitz, U; Wieland, K; Kakkar, V V; Cooper, D N.

Affiliation

Berg LP; Charter Molecular Genetics Laboratory, Thrombosis Research Institute, London, UK.

Blood Coagul Fibrinolysis ; 5(1): 59-62, 1994 Feb.

Article in En | MEDLINE | ID: mdl-8180339

Subject(s)

Factor XI Deficiency/complications; Hemophilia A/complications; Hemophilia A/genetics; Jews; Base Sequence; Deoxyribonucleases, Type II Site-Specific; Molecular Sequence Data; Mutation; Phenotype; Polymerase Chain Reaction

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Collection: 01-internacional Database: MEDLINE Main subject: Jews / Factor XI Deficiency / Hemophilia A Type of study: Prognostic_studies Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 1994 Type: Article Affiliation country: United kingdom

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