Frequency of HFE gene mutations and genotype-phenotype correlations in Swiss patients with hereditary haemochromatosis;Haufigkeit der HFE-genmutationen und genotyp-phanotyp-beziehungen bei patienten mit hereditarer hamochromatose in der Schweiz

Schweizerische Medizinische Wochenschrift

Volumn 130, Issue 31-32, 2000, Pages 1112-1119

  Himmelmann, A ^a   Bortoluzzi, L ^a   St Jansen, ^a   Fehr, J ^a  

^a Stadtspital Triemli Departement fur Innere Medizin Abteilung fur Gastroenterologie   (Switzerland)

Author keywords

Genetics; Haemochromatosis; Iron body stores; Symptoms

Indexed keywords

IRON; HFE PROTEIN, HUMAN; HLA ANTIGEN; HLA ANTIGEN CLASS 1; MEMBRANE PROTEIN;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE; HEMOCHROMATOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; IRON STORAGE; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; QUESTIONNAIRE; SEX DIFFERENCE; SWEDEN; AMINO ACID SUBSTITUTION; GENE; GENETICS; HETEROZYGOTE DETECTION; HOMOZYGOTE; MIDDLE AGED; POINT MUTATION; SWITZERLAND;

ADULT; AGED; AMINO ACID SUBSTITUTION; FEMALE; GENES, MHC CLASS I; GENOTYPE; HEMOCHROMATOSIS; HETEROZYGOTE DETECTION; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HOMOZYGOTE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; PHENOTYPE; POINT MUTATION; SWITZERLAND;

EID: 0034622438     PISSN: 00367672     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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