Inherited HFE-unrelated hemochromatosis in Italian families

Hepatology

Volumn 29, Issue 5, 1999, Pages 1563-1564

  Camaschella, Clara ^a   Fargion, Silvia ^b   Sampietro, Maurizio ^b   Roetto, Antonella ^a   Bosio, Sandra ^a   Garozzo, Giovanni ^c   Arosio, Cristina ^b   Piperno, Alberto ^b  

^a UNIVERSITY OF TURIN   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c CIVILE M P AREZZO HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; FAMILIAL INCIDENCE; FEMALE; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC RISK; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; IRON OVERLOAD; ITALY; MALE; PHENOTYPE; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; HAPLOTYPES; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HUMANS; IRON; ITALY; MALE; MEMBRANE PROTEINS; MUTATION; PHENOTYPE;

EID: 0032899949     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1002/hep.510290509     Document Type: Article

References (1)

1. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;13:399-408.