Publication | Closed Access
Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency
25
Citations
31
References
2019
Year
Serpinc1 MutationsMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathologyMolecular GeneticsDisease Gene IdentificationMedicineJapanese PatientsClinical GeneticsAntithrombin Deficiency
| Year | Citations | |
|---|---|---|
Page 1
Page 1