Phenotypic and Genotypic Signatures of VWF Exon 18 in Eastern Saudi Patients Previously Diagnosed with Type 1 von Willebrand Disease.

Faisal M AlzahraniAsma A Al FarisLayla A BashawriFathelrahman Mahdi HassanOmar S El-MasryMaryam A AldossaryOsama Al SultanJesu Francis Borgio Mohammed A AlsahliAnne Goodeve

Published in: International journal of general medicine (2022)

gene reported in all groups and the disease status; however, blood group analysis and genome-wide genotyping could help to highlight high-risk groups and improve clinical management of VWD.

Keyphrases

genome wide
dna methylation
end stage renal disease
copy number
ejection fraction
newly diagnosed
chronic kidney disease
prognostic factors
peritoneal dialysis
south africa
high throughput
patient reported outcomes