A novel mutation Gly 1672-->Arg in type 2A and a homozygous mutation in type 2B von Willebrand disease.

Hagiwara, T; Inaba, H; Yoshida, S; Nagaizumi, K; Arai, M; Hanabusa, H; Fukutake, K

Hagiwara, T; Inaba, H; Yoshida, S; Nagaizumi, K; Arai, M; Hanabusa, H; Fukutake, K.

Affiliation

Hagiwara T; Department of Clinical Pathology, Tokyo Medical College, Japan.

Thromb Haemost ; 76(2): 253-7, 1996 Aug.

Article in En | MEDLINE | ID: mdl-8865541

Subject(s)

Arginine/chemistry; Asian People/genetics; Glycine/chemistry; Homozygote; Point Mutation; von Willebrand Diseases/genetics; Case-Control Studies; DNA/genetics; DNA Mutational Analysis; Exons; Humans; Pedigree; Polymerase Chain Reaction; Polymorphism, Genetic

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Database: MEDLINE Main subject: Arginine / Von Willebrand Diseases / Point Mutation / Asian People / Glycine / Homozygote Type of study: Observational_studies / Prognostic_studies Limits: Humans Language: En Year: 1996 Type: Article

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