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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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| Pubblicato in: | Med Arch |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Academy of Medical Sciences of Bosnia and Herzegovina
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7780826/ https://ncbi.nlm.nih.gov/pubmed/33424085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5455/medarh.2020.74.337-341 |
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