Molecular characterization of factor v Leiden G1691A and prothrombin G20210A mutations in Saudi newborns with stroke

Biochemical Genetics

Volumn 49, Issue 9-10, 2011, Pages 601-610

  Gawish, Gihan E H ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

Factor II; Factor V Leiden; Neonatal stroke; Prothrombin

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

ARTICLE; CEREBROVASCULAR ACCIDENT; CONTROLLED STUDY; GENE MUTATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MULTIPLEX POLYMERASE CHAIN REACTION; NEWBORN; RISK FACTOR; SAUDI ARABIA;

BLOOD COAGULATION DISORDERS; CEREBRAL PALSY; FACTOR V; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENOTYPE; HUMANS; INFANT, NEWBORN; INTRACRANIAL HEMORRHAGES; INTRACRANIAL THROMBOSIS; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTHROMBIN; SAUDI ARABIA; SEQUENCE ANALYSIS, DNA; STROKE;

EID: 80054749989     PISSN: 00062928     EISSN: 15734927     Source Type: Journal    
DOI: 10.1007/s10528-011-9435-7     Document Type: Article

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