Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362→Thr (Prothrombin Vellore 1) mutation - Concepedia

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Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362→Thr (Prothrombin Vellore 1) mutation

DOI Full Paper Access

17

Citations

29

References

2005

Year

Giridhara R. Jayandharan, Auro Viswabandya, S. Baidya, Sukesh C. Nair, Shaji R Velayudhan, Mammen Chandy, Alok Srivastava

Journal of Thrombosis and Haemostasis

Indian PatientsAllelic VariantGenetic DisorderGeneticsInherited Metabolic DiseaseHematologyHereditary Prothrombin DeficiencyPathologyHuman PolymorphismProthrombin Vellore 1MedicineClinical Genetics

References

	Year	Citations

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