Screening for hemochromatosis: Patients with liver disease, families, and populations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11894-004-0025-2.pdf
Reference51 articles.
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2. Simon M, Bourel M, Fauchet R, et al.: Idiopathic haemochromatosis: demonstration of recessive transmission and early detection by family HLA typing. N Engl J Med 1977, 297:1017–1021.
3. Feder JN, Gnirke A, Thomas W, et al.: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996,13:399–409.
4. Olynyk JK: Hereditary haemochromatosis: diagnosis and management in the gene era. Liver 1999, 19:73–80.
5. Bomford A: Genetics of hemochromatosis. Lancet 2002,360:1673–1681. This paper offers a comprehensive review of the genes mutated in hereditary hemochromatosis, prevalence of HFE mutations, and penetrance of the disease.
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