Clinical consequences of iron overload in hemochromatosis homozygotes

Blood

Volumn 101, Issue 9, 2003, Pages 3351-3357

  Ajioka, Richard S ^c   Kushner, James P ^a   Beutler, Ernest ^b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c Dept of Molec and Exp Medicine ^*

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; BLOOD DONOR; EUROPE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; INCIDENCE; IRON OVERLOAD; LIVER BIOPSY; MORBIDITY; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RETROSPECTIVE STUDY; REVIEW; ADULT; AGE DISTRIBUTION; AGED; AMINO ACID SUBSTITUTION; BLOOD; CODON; EPIDEMIOLOGY; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE; MASS SCREENING; MIDDLE AGED; MISSENSE MUTATION; NORWAY; OBSERVER VARIATION; PATHOLOGY; PENETRANCE; PHLEBOTOMY; POINT MUTATION; UNITED STATES;

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

ADULT; AGE DISTRIBUTION; AGED; AMINO ACID SUBSTITUTION; BLOOD DONORS; CALIFORNIA; CODON; FEMALE; FERRITINS; GENETIC PREDISPOSITION TO DISEASE; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HOMOZYGOTE; HUMANS; IRON; IRON OVERLOAD; MALE; MASS SCREENING; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION, MISSENSE; NORWAY; OBSERVER VARIATION; PENETRANCE; PHLEBOTOMY; POINT MUTATION; SELECTION BIAS; TRANSFERRIN;

EID: 0038542811     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2002-11-3453     Document Type: Review

References (0)