c.1058C>T variant in the SERPINC1 gene is pathogenic for antithrombin deficiency
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Overview
status
publication date
- July 2015
has subject area
- 1102 Cardiorespiratory Medicine and Haematology (FoR)
- Adult (MeSH)
- Antithrombin III (MeSH)
- Antithrombin III Deficiency (MeSH)
- Base Sequence (MeSH)
- Blood Coagulation (MeSH)
- Female (MeSH)
- Genetic Predisposition to Disease (MeSH)
- Genotype (MeSH)
- Humans (MeSH)
- Immunology (Science Metrix)
- Infant (MeSH)
- Male (MeSH)
- Mutation (MeSH)
- Phenotype (MeSH)
published in
- British Journal of Haematology Journal