Publication | Closed Access
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency
29
Citations
27
References
2009
Year
Mendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseLarge Serpinc1 DeletionsPathologyMolecular GeneticsDisease Gene IdentificationMedicineVariant InterpretationClinical GeneticsAntithrombin Deficiency
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