Found: 4
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High protein S activity due to C4b‐binding protein deficiency in a 34‐year‐old Surinamese female with ischemic retinopathy.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
SERPINC1 gene mutations in antithrombin deficiency.
- Published in:
- British Journal of Haematology, 2017, v. 178, n. 2, p. 279, doi. 10.1111/bjh.14658
- By:
- Publication type:
- Article
Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples.
- Published in:
- International Journal of Laboratory Hematology, 2021, v. 43, n. 3, p. e101, doi. 10.1111/ijlh.13390
- By:
- Publication type:
- Article