Fibrinogen Córdoba: Biochemical characterization of a new congenital hypodysfibrinogenemia [2]

Clinica Chimica Acta

Volumn 317, Issue 1-2, 2002, Pages 239-240

  Quiñonez, Mariela ^a   Fernández, Eduardo ^a   Guglielmone, Hugo A ^a,b   Sánchez, María C ^b  

^a Lab Analisis Clinicos E   (Argentina)

^b UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

BATROXOBIN; CORDOBA FIBRINOGEN; FIBRIN; FIBRIN MONOMER; FIBRINOGEN; THROMBIN; UNCLASSIFIED DRUG;

ADULT; BLOOD CHEMISTRY; BLOOD CLOTTING DISORDER; CASE REPORT; CLINICAL FEATURE; CONGENITAL HYPODYSFIBRINOGENEMIA; DISEASE CLASSIFICATION; FIBRIN POLYMERIZATION; FIBRINOGEN BLOOD LEVEL; FIBRINOGEN DEFECT; HUMAN; IMMUNOASSAY; LETTER; MALE; MOLECULAR WEIGHT; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION; THROMBIN TIME; TURBIDITY;

AFIBRINOGENEMIA; FEMALE; FIBRINOGENS, ABNORMAL; HUMANS; MALE;

EID: 0036152806     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-8981(01)00780-X     Document Type: Letter

References (4)

1. Structure and function of fibrinogen inferred from hereditary dysfibrinogens
2. Congenital dysfibrinogenemia
3. Fibrinogen Petoskey: Identification of a new dysfribrinogenemia characterized by altered release of fibrinopeptide A