Thrombotic events in compound heterozygotes for a high affinity hemoglobin variant: Hb Milledgeville [α44(CE2)Pro →Leu (α2)] and factor V Leiden

Hemoglobin

Volumn 26, Issue 3, 2002, Pages 285-290

  Hanss, Michel ^a   Lacan, Philippe ^a   Aubry, Martine ^a   Lienhard, Anne ^a   Francina, Alain ^a  

^a EDOUARD HERRIOT HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG; BLOOD CLOTTING FACTOR 5;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; BLOOD VISCOSITY; BONE MARROW BIOPSY; CLINICAL ARTICLE; ECHOGRAPHY; ERYTHROCYTOSIS; FEMALE; GENE MUTATION; HEMOGLOBIN MILLEDGEVILLE; HETEROZYGOTE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; ISOELECTRIC FOCUSING; MALE; MULTIGENE FAMILY; RECEPTOR AFFINITY; THROMBOSIS; BLOOD; CASE REPORT; FAMILY HEALTH; FRANCE; GENETIC VARIABILITY; GENETICS; HEMOGLOBINOPATHY; MIDDLE AGED; PHYSIOLOGY; VEIN THROMBOSIS;

AGED; AMINO ACID SUBSTITUTION; FACTOR V; FAMILY HEALTH; FEMALE; FRANCE; HEMOGLOBINOPATHIES; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; VARIATION (GENETICS); VENOUS THROMBOSIS;

EID: 0036402721     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-120015032     Document Type: Article

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