Resolving Differential Diagnostic Problems in Von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing

Reka Gindele,Adrienne Kerenyi,Judit Kallai,Gyorgy Pfliegler,Agota Schlammadinger,Istvan Szegedi,Tamas Major,Zsuzsanna Szabo,Zsuzsa Bagoly,Csongor Kiss,Janos Kappelmayer,Zsuzsanna Bereczky

Life（2021）

引用 3|浏览29

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next generation sequencing,rare bleeding disorders,von Willebrand disease,hemophilia A,hereditary hemorrhagic telangiectasia,differential diagnosis,prekallikrein deficiency,APTT prolongation

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