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）

Cited 4|Views29

Key words

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

AI Read Science

Must-Reading Tree

Example

Generate MRT to find the research sequence of this paper

Chat Paper

Summary is being generated by the instructions you defined