Associated Papers
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
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
Bell S et al.
Communications Biology, 2021
33536631 (PubMed )
Supplement: 42003_2020_1575_MOESM4_ESM.xlsx › Supplementary_Data_10
Association between human prothrombin variant (T165M) and kidney stone disease.
Rungroj N et al.
Plos One, 2012
Select a paper to view details