Author:
Barton James C,Acton Ronald T
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference49 articles.
1. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo Jr R, Ellis MC, Fullan A, et al: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996, 13: 399-408.
2. Simon M, Le Mignon L, Fauchet R, Yaouanq J, David V, Edan G, Bourel M: A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a homozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association. Am J Hum Genet. 1987, 41: 89-105.
3. Fairbanks VF: Hemochromatosis: population genetics. In: Hemochromatosis. Genetics, Pathophysiology, Diagnosis, and Treatment. Edited by: Barton JC, Edwards CQ. 2000, Cambridge, Cambridge University Press, 42-50.
4. Jazwinska EC: The ancestral haplotype in hemochromatosis. In: Hemochromatosis. Genetics, Pathophysiology, Diagnosis, and Treatment. Edited by: Barton JC, Edwards CQ. 2000, Cambridge, Cambridge University Press, 91-99.
5. Porto G, de Sousa M: Variation in hemochromatosis prevalence and genotype in national groups. In: Hemochromatosis. Genetics, Pathophysiology, Diagnosis, and Treatment. Edited by: Barton JC, Edwards CQ. 2000, Cambridge, Cambridge University Press, 51-62.
Cited by
27 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献