Haemochromatosis in patients with β-thalassaemia trait

British Journal of Haematology

Volumn 111, Issue 3, 2000, Pages 908-914

  Piperno, Alberto ^a   Mariani, Raffaella ^a   Arosio, Cristina ^b   Vergani, Anna ^a   Bosio, Sandra ^c   Fargion, Silvia ^d   Sampietro, Maurizio ^d   Girelli, Domenico ^e   Fraquelli, Mirella ^d   Conte, Dario ^d   Fiorelli, Gemino ^d   Camaschella, Clara ^c  

^a SAN GERARDO HOSPITAL   (Italy)

^b ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^c UNIVERSITY OF TURIN   (Italy)

^d UNIVERSITY OF MILAN   (Italy)

^e UNIVERSITY OF VERONA   (Italy)

Author keywords

thalassaemia; Haemochromatosis; HFE; Ineffective erythropoiesis; Iron overload

Indexed keywords

IRON;

ADULT; AGED; ALLELISM; ARTICLE; BETA THALASSEMIA; CHROMOSOME 1Q; CHROMOSOME 6P; CLINICAL ARTICLE; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; FEMALE; HEMOCHROMATOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; IRON BLOOD LEVEL; IRON OVERLOAD; MALE; PHENOTYPE; PRIORITY JOURNAL;

ADULT; BETA-THALASSEMIA; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; HAPLOTYPES; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HUMANS; LIVER; MALE; MEMBRANE PROTEINS; MIDDLE AGED; PEDIGREE; STATISTICS, NONPARAMETRIC;

EID: 0034493507     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2000.02436.x     Document Type: Article

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