Low prevalence of coagulation F2 and F5 polymorphisms in mothers and children in a large cohort of patients with neonatal arterial ischemic stroke: Correspondence

British Journal of Haematology

Volumn 150, Issue 6, 2010, Pages 709-712

  Renaud, C ^a,b   Tardy Poncet, B ^a,b,c   Presles, E ^a,b   Chabrier, S ^a,c  

^a INSERM   (France)

^b University Jean Monnet of Saint Etienne EA3065   (France)

^c HÔPITAL NORD   (France)

Author keywords

F2 G20210A mutation; F5 R506Q (factor V Leiden); neonatal stroke

Indexed keywords

BLOOD CLOTTING FACTOR 5; PROTHROMBIN;

BRAIN ISCHEMIA; CHILDHOOD DISEASE; DNA POLYMORPHISM; GENE MUTATION; GENETIC ANALYSIS; GENETIC RISK; HUMAN; LABORATORY TEST; LETTER; PREVALENCE; PRIORITY JOURNAL; THROMBOPHILIA;

BRAIN ISCHEMIA; COHORT STUDIES; FACTOR V; FEMALE; HUMANS; INFANT, NEWBORN; POLYMORPHISM, GENETIC; PROTHROMBIN; STROKE;

EID: 77956316211     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2010.08259.x     Document Type: Letter

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