Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

Journal of Clinical Investigation

Volumn 108, Issue 4, 2001, Pages 619-623

  Montosi, G ^a   Donovan, A ^a   Totaro, A ^a   Garuti, C ^a   Pignatti, E ^a   Cassanelli, S ^a   Trenor, C C ^a   Gasparini, P ^a   Andrews, N C ^a   Pietrangelo, A ^a  

^a UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FERROPORTIN; IRON BINDING PROTEIN; MUTANT PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2Q; HEMOCHROMATOSIS; HUMAN; IRON STORAGE; MISSENSE MUTATION; PRIORITY JOURNAL;

AMINO ACID SUBSTITUTION; ANIMALS; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; CHROMOSOMES, HUMAN, PAIR 2; CODON; EXONS; FEMALE; GENES, DOMINANT; GENETIC HETEROGENEITY; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; HOMEOSTASIS; HUMANS; IRON; IRON OVERLOAD; ITALY; LOD SCORE; MALE; MEMBRANE PROTEINS; MICE; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; RECEPTORS, TRANSFERRIN; RETICULOENDOTHELIAL SYSTEM;

EID: 17944380796     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI200113468     Document Type: Article

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