Molecular Pathogenesis of Hemochromatosis
Author:
Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4613-0391-6_80.pdf
Reference24 articles.
1. Simon M, Bourel M, Genetet B, Fauchet R: Idiopathic hemochromatosis: demonstration of recessive transmission and early detection by family HLA typing. N Engl J Med 297: 1017–1021, 1977.
2. Niederau C, Fischer R, Sonnenberg A, Stremmel W, Trampisch HJ, Strohmeyer G: Survival and causes of death in cirrhotic and non cirrhotic patients with primary hemochromatosis. N Engl J Med 313:1256–1262, 1985.
3. Edwards CQ, Griffin LM, Goldgar D, Drummond C, Skolnick M, Kushner J: Prevalence of hemochromatosis among 11.065 presumably healthy blood donors. New Engl J Med 318: 1355–1362, 1988.
4. Dadone MM, Kushner JP, Edwards CQ, Bishop DT, Skolnick MH: Hereditary hemochromatosis: analysis of laboratory expression of the disease by genotype in 18 pedigrees. Am J Clin Pathol 78: 196–207, 1982.
5. Edwards CQ, Kushner JP: Current Concepts: Screening for Hemochromatosis. New Engl J Med 328: 1616–1620, 1993.
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