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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, 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. Feder JN, et al. Nat Genet. 1996 Aug;13(4):399-408. doi: 10.1038/ng0896-399. Nat Genet. 1996. PMID: 8696333
The discovery of the new haemochromatosis gene. 1996.
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A. Feder JN, et al. J Hepatol. 2003 Jun;38(6):704-9. doi: 10.1016/s0168-8278(03)00142-9. J Hepatol. 2003. PMID: 12763361 No abstract available.
Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.
Waheed A, Parkkila S, Zhou XY, Tomatsu S, Tsuchihashi Z, Feder JN, Schatzman RC, Britton RS, Bacon BR, Sly WS. Waheed A, et al. Among authors: feder jn. Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12384-9. doi: 10.1073/pnas.94.23.12384. Proc Natl Acad Sci U S A. 1997. PMID: 9356458 Free PMC article.
82 results