HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls

European Journal of Human Genetics

Volumn 9, Issue 12, 2001, Pages 961-964

  de Juan, Ma Dolores ^a   Reta, Ana ^a   Castiella, Agustin ^b   Pozueta, Jasone ^a   Prada, Alvaro ^a   Cuadrado, Emilio ^a  

^a HOSPITAL DONOSTIA   (Spain)

^b HOSPITAL DE MENDARO   (Spain)

Author keywords

H63D mutation; Haemochromatosis; HFE gene

Indexed keywords

ASPARTIC ACID; CYSTEINE; HISTIDINE; HLA A ANTIGEN; HLA B ANTIGEN; TYROSINE;

ADULT; AGED; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE; HEMOCHROMATOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INCIDENCE; IRON OVERLOAD; MALE; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; SPAIN;

ADULT; AGED; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; PREVALENCE; SPAIN;

EID: 0035712326     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200731     Document Type: Article

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