Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency

Blood

Volumn 93, Issue 7, 1999, Pages 2253-2260

  Neerman Arbez, M ^b   Johnson, K M ^b   Morris, M A ^b   McVey, J H ^b   Peyvandi, F ^b   Nichols, W C ^b   Ginsburg, D ^b   Rossier, C ^b   Antonarakis, S E ^b   Tuddenham, E G D ^a  

^a IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLOOD CLOTTING FACTOR 5 DEFICIENCY; CODON; COMORBIDITY; FRAMESHIFT MUTATION; GENE DELETION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEMOPHILIA A; HUMAN; IMMUNOBLOTTING; MAJOR CLINICAL STUDY; NONSENSE MUTATION; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN SYNTHESIS REGULATION; SEQUENCE ANALYSIS; SITE DIRECTED MUTAGENESIS; TRANSLATION INITIATION;

ALGERIA; ALLELES; CHINA; CODON; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; ETHNIC GROUPS; FACTOR V DEFICIENCY; FEMALE; GENES, RECESSIVE; GREAT BRITAIN; HAPLOTYPES; HEMOPHILIA A; HUMANS; IRAN; ITALY; JEWS; MALE; MANNOSE-BINDING LECTINS; MEMBRANE PROTEINS; MUTATION; PAKISTAN; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SOUTH AFRICA;

EID: 0033120708     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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