KASP-PCR method to screen thrombophilia genetic risk factors
Reham Altwayan, Hüseyin Tombuloğlu, Abdulrahman Alhusil, Taghreed Awadh, Mona Altwayan, Heba Albaqawi, Noof Aldossary, Turgay Ünver
This study develops a KASP-PCR panel to detect thrombophilia-associated SNPs, finding that 86.5% of patients have at least one mutation and seven have three mutations.
medRxiv · Oct 25, 2023 · PreprintGenetic & Genomic Medicine