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2. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components. Alvarez V, Coto E, Setién F, Spath PJ, López-Larrea C. Am J Med Genet; 1995 Feb 13; 55(4):408-13. PubMed ID: 7762578 [Abstract] [Full Text] [Related]
3. Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies. Fernie BA, Würzner R, Orren A, Morgan BP, Potter PC, Platonov AE, Vershinina IV, Shipulin GA, Lachmann PJ, Hobart MJ. J Immunol; 1996 Oct 15; 157(8):3648-57. PubMed ID: 8871666 [Abstract] [Full Text] [Related]
7. DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13. Fernie BA, Orren A, Schlesinger M, Würzner R, Platonov AE, Cooper RC, Williams YE, Hobart MJ. Ann Hum Genet; 1997 Jul 15; 61(Pt 4):287-98. PubMed ID: 9365782 [Abstract] [Full Text] [Related]
10. Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement. Potter PC, Warburton C, Würzner R, Orren A, Di Scipio R. Exp Clin Immunogenet; 1993 Jul 15; 10(1):38-44. PubMed ID: 7691111 [Abstract] [Full Text] [Related]
18. Inherited deficiency of the sixth component of complement: a silent or null gene. Glass D, Raum D, Balavitch D, Kagan E, Rabson A, Schur PH, Alper CA. J Immunol; 1978 Feb 15; 120(2):538-41. PubMed ID: 621392 [Abstract] [Full Text] [Related]
19. Inherited deficiency of the seventh component of complement associated with nephritis. Propensity to formation of C56 and related C7-consuming activity. Nemerow GR, Gewurz H, Osofsky SG, Lint TF. J Clin Invest; 1978 Jun 15; 61(6):1602-10. PubMed ID: 350902 [Abstract] [Full Text] [Related]