Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N

Haemophilia

Volumn 12, Issue 4, 2006, Pages 398-400

  Berber, E ^a   Fidanci, I D ^a   Un, C ^b   El Maarri, O ^c   Aktuglu, G ^c   Gurgey, A ^d   Celkan, T ^e   Meral, A ^f   Oldenburg, J ^c   Graw, J ^b   Akar, N ^g   Caglayan, Hande ^a  

^a BOGAZICI UNIVERSITY   (Turkey)

^b Institute of Developmental Genetics   (Turkey)

^c Institute of Experimental Haematology and Transfusion Medicine   (Germany)

^d ISTANBUL UNIVERSITY   (Turkey)

^e HACETTEPE UNIVERSITY   (Turkey)

^f ULUDAG UNIVERSITY   (Turkey)

^g ANKARA UNIVERSITY   (Turkey)

Author keywords

DNA sequencing; FactorVIII; Haemophilia; Mutation detection; Rediagnosis; vWD 2N

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ARTICLE; DIFFERENTIAL DIAGNOSIS; GENETIC POLYMORPHISM; GENETICS; HEMOPHILIA A; HUMAN; INTRON; MALE; MUTATION; NUCLEOTIDE SEQUENCE; VON WILLEBRAND DISEASE;

DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; FACTOR VIII; HEMOPHILIA A; HUMANS; INTRONS; MALE; MUTATION; POLYMORPHISM, GENETIC; VON WILLEBRAND DISEASE;

EID: 34248535395     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2006.01302.x     Document Type: Article

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