Hemochromatosis: Advances in molecular genetics and clinical diagnosis

Journal of Clinical Gastroenterology

Volumn 27, Issue 1, 1998, Pages 41-46

  Bacon, Bruce R ^a  

^a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Hereditary hemochromatosis; Human leukocyte antigen

Indexed keywords

HLA ANTIGEN; IRON;

CLINICAL FEATURE; GASTROINTESTINAL MUCOSA; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HUMAN; IRON ABSORPTION; IRON METABOLISM; IRON OVERLOAD; LIVER DISEASE; MAJOR CLINICAL STUDY; PHLEBOTOMY; PRIORITY JOURNAL; REVIEW;

ALGORITHMS; HEMOCHROMATOSIS; HUMANS; MOLECULAR BIOLOGY; MUTATION;

EID: 0031823535     PISSN: 01920790     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004836-199807000-00008     Document Type: Review

References (5)

1. Trousseau A. Glycosurie: diabete sucre. Clinique Medicale de l'Hotel-Dieu de Paris, vol 2 (ed 2). Paris: Balliere, 1865:663.
2. Von Recklinghausen, FD. Uber Hamochromatose. Tagebl Versamml Natur Artze Heidelberg 1889;62:324.
3. Sheldon JH. Haemochromatosis. London: Oxford University Press, 1935.
4. Simon M, Bourel M, Genetet B, et al. Idiopathic Hemochromatosis: demonstration of recessive transmission and early detection by family HLA typing. N Engl J Med 1977;297:1017.
5. Bacon BR, Tavill AS. Hemochromatosis and iron overload syndromes. In: Zakim D, Boyer TD, eds. Hepatology. A textbook of liver disease. Philadelphia: Saunders, 1996:1439-72.