Hematologically important mutations: Iron storage diseases

Blood Cells, Molecules, and Diseases

Volumn 33, Issue 1, 2004, Pages 40-44

  Beutler, Lisa ^a   Beutler, Ernest ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Gene mutations; HLA; Iron storage disease

Indexed keywords

COMPLEMENTARY DNA; FERROPORTIN 1; HEMOJUVELIN; HEPCIDIN; HFE PROTEIN; IRON; PROTEIN; RECEPTOR SUBTYPE; TRANSFERRIN; TRANSFERRIN RECEPTOR 2; UNCLASSIFIED DRUG;

ARTICLE; GENE MUTATION; HEMATOLOGIC DISEASE; HOMEOSTASIS; HUMAN; MUTATIONAL ANALYSIS; PHENOTYPE; PRIORITY JOURNAL;

DATABASES, FACTUAL; HUMANS; IRON METABOLISM DISORDERS; METAL METABOLISM, INBORN ERRORS; MUTATION; PHENOTYPE;

EID: 3042613923     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2004.03.002     Document Type: Article

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