Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First report from India

Thrombosis and Haemostasis

Volumn 101, Issue 4, 2009, Pages 785-787

  Pai, Navin ^a   Shetty, Shrimati ^a   Idicula Thomas, Susan ^b   Kulkarni, Bipin ^a   Ghosh, Kanjaksha ^a  

^a KEM HOSPITAL   (India)

^b NATIONAL INSTITUTE FOR RESEARCH IN REPRODUCTIVE HEALTH   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

ADOLESCENT; ADULT; CLINICAL ARTICLE; CONTROLLED STUDY; DEEP VEIN THROMBOSIS; DNA DETERMINATION; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; FRAMESHIFT MUTATION; GEL ELECTROPHORESIS; GENETIC POLYMORPHISM; HEREDITY; HUMAN; INDIA; LETTER; MALE; MUTATION; PHENOTYPE; POLYMERASE CHAIN REACTION; PORTAL VEIN OBSTRUCTION; PREVALENCE; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; SAGITTAL SINUS THROMBOSIS; THROMBOPHILIA; THROMBOSIS; X RAY CRYSTALLOGRAPHY;

ADOLESCENT; ADULT; BLOOD COAGULATION; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; FRAMESHIFT MUTATION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INDIA; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; PROTEIN C; PROTEIN C DEFICIENCY; RISK FACTORS; VENOUS THROMBOSIS;

EID: 64849098004     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH08-11-0725     Document Type: Letter

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