Molecular analysis of multiple genetic variants in Spanish FXII-deficient families

Haematologica

Volumn 92, Issue 11, 2007, Pages 1569-1572

  Mordillo, Carolina ^a   Martinez Marchán, Elisabeth ^a   Fontcuberta, Jordi ^a   Soria, José Manuel ^a  

^a HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

C46T; F12 gene; FXII deficiency; SNPs

Indexed keywords

BLOOD CLOTTING FACTOR 7; DNA; MESSENGER RNA;

ADOLESCENT; ADULT; ARTICLE; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CLINICAL ARTICLE; DNA SEQUENCE; EXON; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENETIC VARIABILITY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INTRON; MALE; MOLECULAR GENETICS; MUTATIONAL ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN;

CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; FACTOR XII; FACTOR XII DEFICIENCY; FAMILY HEALTH; GENETIC VARIATION; MUTATION; RNA, MESSENGER; SPAIN;

EID: 36348949734     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: 10.3324/haematol.11388     Document Type: Article

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