Found: 2
Select item for more details and to access through your institution.
Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency.
- Published in:
- International Journal of Hematology, 2023, v. 117, n. 4, p. 523, doi. 10.1007/s12185-022-03509-3
- By:
- Publication type:
- Article
Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.
- Published in:
- 2020
- By:
- Publication type:
- journal article