Role of genetic testing and liver biopsy in the diagnosis of hemochromatosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11894-999-0083-6.pdf
Reference18 articles.
1. Feder JN, Gnirke A, Thomas W, et al.: A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis. Nat Genet 1996, 13:399–408. This is the original paper describing the discovery of the hemochromatosis gene.
2. Zhou XY, Tomatsu S, Fleming R, et al.: HFE gene knockout produces mouse model of hereditary hemochromatosis. Proc Natl Acad Sci 1998, 95:2492–2497.
3. Merryweather-Clarke A, Pointon J, Sherman J, Robson K: Global prevalence of putative haemochromatosis mutations. J Med Genet 1997, 34:275–278.
4. Niederau C, Niederau CM, Lange S, et al.: Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany Ann Intern Med 1998, 128:337–345.
5. Ludwig J, Hashimoto E, Porayko M, et al.: Hemosiderosis in cirrhosis: a study of 447 native livers. Gastroenterology 1997, 112:882–888.
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