- A Novel Missense Mutation Asp506Gly in Exon 13 of the F11 Gene in an Asymptomatic Korean Woman with Mild Factor XI Deficiency
-
Lee JH, Cho HS, Hyun MS, Kim HY, Kim HJ
- KMID: 1781695
- Korean J Lab Med.
- 2011 Oct;31(4):290-293.
- doi: 10.3343/kjlm.2011.31.4.290
Factor XI (FXI) deficiency is a rare autosomal recessive coagulation disorder most commonly found in Ashkenazi and Iraqi Jews, but it is also found in other ethnic groups. It is... -
- CITED
-
- Close
- SHARE
-
- Close
