Association between Genetic Polymorphism and Risk of von Willebrand Disease in Pakistan

von Willebrand disease (VWD) is an inherited, genetically and clinically heterogeneous hemorrhagic disorder. The most common cause of this disease is mutation in the gene that encodes protein von Willebrand factor (VWF) which is responsible for blood clotting. The current study was designed to inves...

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Detalles Bibliográficos
Autores principales: Arshad, Najma, Nawaz, Syed Kashif, Iqbal, Riffat, Arshad, Muhammad, Musheer, Farhana, Naz, Amber, Mushtaq, Iqra, Jaleel, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750513/
https://www.ncbi.nlm.nih.gov/pubmed/29423401
http://dx.doi.org/10.1155/2017/1070471

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750513/
https://www.ncbi.nlm.nih.gov/pubmed/29423401
http://dx.doi.org/10.1155/2017/1070471

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