Is there a 'Basque' profile regarding autosomal recessive deficiencies of coagulation factors?

Haemophilia

Volumn 10, Issue 3, 2004, Pages 276-279

  Bauduer, Frédéric ^a,b   Ducout, L ^a   Dutour, O ^b   Degioanni, A ^b  

^a CENTRE HOSPITALIER DE LA CÔTE BASQUE   (France)

^b AIX MARSEILLE UNIVERSITY   (France)

Author keywords

Basques; Coagulation factors deficiencies; Factor XI deficiency; Population genetics

Indexed keywords

BLOOD CLOTTING FACTOR; BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 12; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; PROTHROMBIN;

ADOLESCENT; ADULT; AFIBRINOGENEMIA; AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 12 DEFICIENCY; BLOOD CLOTTING FACTOR 13 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; BLOOD CLOTTING FACTOR DEFICIENCY; CHILD; COMORBIDITY; FEMALE; FRANCE; GENETIC VARIABILITY; GEOGRAPHIC DISTRIBUTION; HEMOPHILIA; HEMOPHILIA A; HUMAN; INDIVIDUALIZATION; INFANT; MAJOR CLINICAL STUDY; MALE; POPULATION GENETICS; PREVALENCE; PRIORITY JOURNAL; PROTHROMBIN DEFICIENCY; VON WILLEBRAND DISEASE;

EID: 2342536397     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2004.00892.x     Document Type: Article

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