Significance of F8 missense mutations with respect to inhibitor formation.

Schwaab, Rainer; Pavlova, Anna; Albert, Thilo; Caspers, Michael; Oldenburg, Johannes

Schwaab, Rainer; Pavlova, Anna; Albert, Thilo; Caspers, Michael; Oldenburg, Johannes.

Affiliation

Schwaab R; Institute of Experimental Haematology and Transfusion Medicine, University Clinics Bonn, Sigmund-Freud-Str. 25, 53127 Bonn, Germany. Rainer.Schwaab@ukb.uni-bonn.de

Thromb Haemost ; 109(3): 464-70, 2013 Mar.

Article in En | MEDLINE | ID: mdl-23306409

Subject(s)

Factor VIII/antagonists & inhibitors; Factor VIII/genetics; Hemophilia A/genetics; Mutation, Missense; Blood Coagulation Factor Inhibitors/genetics; Codon; DNA Mutational Analysis; DNA, Complementary/metabolism; Humans; Mutation; Phenotype; Point Mutation; Protein Interaction Domains and Motifs

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor VIII / Mutation, Missense / Hemophilia A Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Thromb Haemost Year: 2013 Document type: Article Affiliation country: Germany Country of publication: Germany

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