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Phenotypic and genotypic (exon 28) characterization of patients diagnosed with von Willebrand disease type 1 in Eastern Saudi Arabia

Von Willebrand factor (VWF) is a plasma glycoprotein that plays a key role in hemostasis. Mutations in this protein can result in von Willebrand disease (VWD), the most common form of bleeding disorder in humans. Patients with type 1 VWD have a quantitative plasmatic deficiency of normal structural...

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Detalles Bibliográficos
Autores principales: Alzahrani, Faisal Mousa, Al Faris, Asma Abdulrazaq, Shaikh, Saeed Sattar, Hassan, Fathelrahman Mahdi, Aldossary, Maryam Ahmed, Al Sultan, Osama, Elhadi, Nasreldin, Alabsi, Sulaiman Salman, Alsahli, Mohammed, Bashawri, Layla Abdulmohsen, Muzaheed, Muzaheed, Goodeve, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165513/
https://www.ncbi.nlm.nih.gov/pubmed/37168293
http://dx.doi.org/10.25122/jml-2022-0276

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