The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype

Human Molecular Genetics

Volumn 13, Issue 17, 2004, Pages 1913-1918

  Le Gac, Gérald ^a,b   Scotet, Virginie ^a   Ka, Chandran ^a,c   Gourlaouen, Isabelle ^b   Bryckaert, Laurence ^b   Jacolot, Sandrine ^a,c   Mura, Catherine ^a,c   Férec, Claude ^a,b,c  

^a INSERM   (France)

^b ETABLISSEMENT FRANÇAIS DU SANG   (France)

^c UNIVERSITÉ DE BRETAGNE OCCIDENTALE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ASPARAGINE; ASPARTIC ACID; CYSTEINE; FERRITIN; GLUTAMIC ACID; GLUTAMINE; GLYCINE; LEUCINE; LYSINE; PROLINE; SERINE; TYROSINE; VALINE;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; FERRITIN BLOOD LEVEL; GENETIC ASSOCIATION; GENETIC CODE; GENETIC IDENTIFICATION; GENETIC RISK; HEMOCHROMATOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; IRON OVERLOAD; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; STUDENT T TEST;

DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; FERRITINS; FRANCE; GENOTYPE; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION, MISSENSE; PHENOTYPE; SEQUENCE ANALYSIS, DNA; TRANSFERRIN;

EID: 4544314123     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddh206     Document Type: Article

References (21)

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