Associated Papers
Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk.
Alkhamis FA et al.
Functional & Integrative Genomics, 2023
36973604 (PubMed )
Supplement: 10142_2023_1039_MOESM1_ESM.xlsx › all_variants
A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene.
Mansory EM et al.
Research and Practice in Thrombosis and Haemostasis, 2021
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