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Journal Abstract Search

131 related items for PubMed ID: 7508350

  • 1. C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP).
    Fernie BA, Hobart MJ, Delbridge G, Potter PC, Orren A, Lachmann PJ.
    Clin Exp Immunol; 1994 Feb; 95(2):351-6. PubMed ID: 7508350
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  • 3. Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency.
    Orren A, Würzner R, Potter PC, Fernie BA, Coetzee S, Morgan BP, Lachmann PJ.
    Immunology; 1992 Jan; 75(1):10-6. PubMed ID: 1537585
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  • 8. MspI polymorphism at the human complement component C6 gene (C6).
    Coto E, Domínguez O, Martínez-Naves E, Setién F, Gutiérrez V, López-Larrea C.
    Nucleic Acids Res; 1991 Jan 11; 19(1):194. PubMed ID: 1707160
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  • 10. Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.
    Dewald G, Nöthen MM, Cichon S.
    Biochem Biophys Res Commun; 1993 Jul 15; 194(1):458-64. PubMed ID: 8101442
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  • 15. Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family.
    Parham KL, Roberts A, Thomas A, Würzner R, Henderson HE, Potter PC, Morgan BP, Orren A.
    Mol Immunol; 2007 Apr 15; 44(10):2756-60. PubMed ID: 17257682
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  • 18. The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.
    Rogne S, Myklebost O, Olving JH, Kyrkjebø HT, Jonassen R, Olaisen B, Gedde-Dahl T.
    J Med Genet; 1991 Sep 15; 28(9):587-90. PubMed ID: 1683409
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