Phenotypic and Genotypic Characterization of von Willebrand Factor Gene (Exon 18 and 20) in Saudi Healthy Individuals

INTRODUCTION: Von Willebrand disease (VWD) is an autosomal congenital bleeding syndrome that was described as being the most widespread genetic condition among men. In Saudi Arabia, the genotyping of the VWF gene is necessary to establish a diagnosis procedure for VWD. AIM: The current research, how...

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Detalles Bibliográficos
Autores principales: Alzahrani, Faisal M., Aldossary, Nemat, Hassan, Fathelrahman Mahdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2020
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780826/
https://www.ncbi.nlm.nih.gov/pubmed/33424085
http://dx.doi.org/10.5455/medarh.2020.74.337-341

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780826/
https://www.ncbi.nlm.nih.gov/pubmed/33424085
http://dx.doi.org/10.5455/medarh.2020.74.337-341

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