A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.

Mansory, Eman M; Bhai, Pratibha; Stuart, Alan; Laudenbach, Lori; Sadikovic, Bekim; Lazo-Langner, Alejandro

Mansory, Eman M; Bhai, Pratibha; Stuart, Alan; Laudenbach, Lori; Sadikovic, Bekim; Lazo-Langner, Alejandro.

Afiliação

Mansory EM; Division of Hematology Department of Medicine Western University London ON Canada.
Bhai P; Department of Hematology King Abdulaziz University Jeddah Saudi Arabia.
Stuart A; Molecular Diagnostics Division Department of Pathology and Laboratory Medicine Western University London ON Canada.
Laudenbach L; Molecular Diagnostics Division Department of Pathology and Laboratory Medicine Western University London ON Canada.
Sadikovic B; Bleeding Disorders Program London Health Sciences Program London ON Canada.
Lazo-Langner A; Molecular Diagnostics Division Department of Pathology and Laboratory Medicine Western University London ON Canada.

Res Pract Thromb Haemost ; 5(4): e12510, 2021 May.

Article em En | MEDLINE | ID: mdl-33977210

Palavras-chave

bleeding disorder; dysprothrombinemia; hypoprothrombinemia; prothrombin deficiency; prothrombin mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2021 Tipo de documento: Article

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