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系统性红斑狼疮与人类白细胞抗原(HLA)基因的关系

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出处 《医学综述》 2003年第10期616-617,共2页 Medical Recapitulate
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  • 2Rupert KL, Rennebohm RM, Yu CY. An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis[J]. Exp Clin Immunogenet,1999, 16( 2) : 81-97.
  • 3Lee SG, Song K. Genomic organization of the human DDX13 gene located between RD and RP1 in the class III MHC complex[J]. Mol Cells, 1997, 7(3): 414-418.
  • 4Peelman LJ, Mattheeuws M, Van-Zeveren A, et al. Conservation of the RD-BF-C2 organization in the pig MHC class-III region: mapping and cloning of the pig RD gene[J]. Anim Genet,1996, 27(1): 35-42.
  • 5WHO-IUlS Nomenclature Sub-Committee. Nomenclature for human complement component C2[J]. Bull World Health Organ, 1992, 70 (4): 527-530.
  • 6WHO-IUlS Nomenclature Sub-Committee.Revised nomenclature for human complement component C4[J]. Bull World Health Organ, 1992, 70 (4): 531-535.
  • 7WHO-IUlS Nomenclature Sub-Committee. Nomenclature for human complement factor B[J]. Bull World Health Organ, 1992, 70 (4): 541-546.
  • 8Lokki ML, Circolo A, Ahokas P, et al.Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes[J]. J Immunol, 1999, 162(6):3687-3693.
  • 9Fredrikson GN, Gullstrand B, Schneider PM, et al.Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon[J]. Hum Immunol, 1998, 59(11): 713-719.
  • 10Naves M, Hajeer AH, Teh-LS, et al.Complement C4B null allele status confers risk for systemic lupus erythematosus in a Spanish population[J]. Eur J Immunogenet, 1998, 25(4): 317-320.

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