Coexistent Hereditary Hemochromatosis and α1-Antitrypsin Deficiency

Archives of Pathology and Laboratory Medicine

Volumn 128, Issue 4, 2004, Pages 491-492

  Shen, Rulong ^a   Frankel, Wendy L ^a   Wen, Ping ^a  

^a THE OHIO STATE UNIVERSITY WEXNER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IRON;

ADULT; ALPHA 1 ANTITRYPSIN DEFICIENCY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANCER RISK; CASE REPORT; CHROMOSOME 14Q; CHROMOSOME 6P; COMORBIDITY; DISEASE EXACERBATION; HEMOCHROMATOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; IRON OVERLOAD; LIVER BIOPSY; LIVER CELL CARCINOMA; MALE; MISSENSE MUTATION;

ALPHA 1-ANTITRYPSIN DEFICIENCY; GENOTYPE; HEMOCHROMATOSIS; HEPATOCYTES; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; INCIDENTAL FINDINGS; IRON OVERLOAD; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION, MISSENSE;

EID: 1842531322     PISSN: 00039985     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

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