Author:
Pacho Arantza,Mancebo Esther,del Rey Manuel J,Castro Maria J,Oliver Desamparados,García-Berciano Miguel,González Luis,Morales Pablo
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference26 articles.
1. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK: A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis. Nat Genet. 1996, 13: 399-408. 10.1038/ng0896-399.
2. Candore G, Mantovani V, Balistreri CR, Lio D, Colonna-Romano G, Cerreta V, Carru C, Deiana L, Pes G, Menardi G, Perotti L, Miotti V, Bevilacqua E, Amoroso A, Caruso C: Frequency of the HFE gene mutations in five Italian populations. Blood Cells Mol Dis. 2002, 29 (3): 267-73. 10.1006/bcmd.2002.0567.
3. Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justio B, Wolff R, De Sousa M: Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis. Immunogenetics. 1998, 47: 404-410. 10.1007/s002510050376.
4. Mura C, Raguenes O, Ferec C: HFE mutations in 711 hemochromatosis probands: evidence for S65C implication in the mild form of hemochromatosis. Blood. 1999, 93: 2502-2505.
5. 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.
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