메뉴 건너뛰기




Volumn 16, Issue 3, 1999, Pages 150-161

Five new polymorphisms in the complement C7 gene and their association with C7 deficiency

Author keywords

C7 deficiency; Complement C7 gene; Polymorphism

Indexed keywords

COMPLEMENT COMPONENT C7;

EID: 0032970944     PISSN: 02549670     EISSN: None     Source Type: Journal    
DOI: 10.1159/000019107     Document Type: Article
Times cited : (4)

References (14)
  • 2
    • 0029876008 scopus 로고    scopus 로고
    • A new intronic polymorphism in the C7 gene 36 bp from the common expressed C7 MN polymorphism
    • Fernie BA, Würzner R, Orren A, Hobart MJ: A new intronic polymorphism in the C7 gene 36 bp from the common expressed C7 MN polymorphism. Ann Hum Genet 1996;60:179-182.
    • (1996) Ann Hum Genet , vol.60 , pp. 179-182
    • Fernie, B.A.1    Würzner, R.2    Orren, A.3    Hobart, M.J.4
  • 6
    • 0031784829 scopus 로고    scopus 로고
    • The molecular bases of c6 deficiency in the Western Cape, Republic of South Africa
    • Hobart MJ, Fernie BA, Fijen APMJ, Orren A: The molecular bases of C6 deficiency in the Western Cape, Republic of South Africa. Hum Genet 1998;103:506-512.
    • (1998) Hum Genet , vol.103 , pp. 506-512
    • Hobart, M.J.1    Fernie, B.A.2    Fijen, A.P.M.J.3    Orren, A.4
  • 8
    • 0030659814 scopus 로고    scopus 로고
    • 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 R, Williams YE, Hobart MJ: 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. Ann Hum Genet 1997;61: 287-298.
    • (1997) Ann Hum Genet , vol.61 , pp. 287-298
    • Fernie, B.A.1    Orren, A.2    Schlesinger, M.3    Würzner, R.4    Platonov, A.E.5    Cooper, R.6    Williams, Y.E.7    Hobart, M.J.8
  • 9
    • 0031754495 scopus 로고    scopus 로고
    • C7 deficiency: Seven further molecular defects and their associated marker haplotypes
    • Fernie BA, Hobart MJ: C7 deficiency: Seven further molecular defects and their associated marker haplotypes. Hum Genet 1998;103:513-519.
    • (1998) Hum Genet , vol.103 , pp. 513-519
    • Fernie, B.A.1    Hobart, M.J.2
  • 10
    • 0018664648 scopus 로고
    • DNA sequence variants in the Gγ-, Aγ- and δ- and β-globin genes in man
    • Jeffreys AJ: DNA sequence variants in the Gγ-, Aγ- and δ- and β-globin genes in man. Cell 1979;18:1-10.
    • (1979) Cell , vol.18 , pp. 1-10
    • Jeffreys, A.J.1
  • 12
    • 0019492995 scopus 로고
    • Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid protein
    • Merril CR, Goldman D, Sedman SA, Ebert MH: Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid protein. Science 1981; 211:1437-1438.
    • (1981) Science , vol.211 , pp. 1437-1438
    • Merril, C.R.1    Goldman, D.2    Sedman, S.A.3    Ebert, M.H.4
  • 13
    • 0021999432 scopus 로고
    • A chi-square test to distinguish allelic association from other causes of phenotypic association between loci
    • Ott J: A chi-square test to distinguish allelic association from other causes of phenotypic association between loci. Genet Epidemiol 1985;2: 79-84.
    • (1985) Genet Epidemiol , vol.2 , pp. 79-84
    • Ott, J.1
  • 14
    • 0026334328 scopus 로고
    • Inherited deficiencies of the terminal components of human complement
    • Würzner R, Orren A, Lachmann PJ: Inherited deficiencies of the terminal components of human complement. Immunodefic Rev 1992;3: 123-147.
    • (1992) Immunodefic Rev , vol.3 , pp. 123-147
    • Würzner, R.1    Orren, A.2    Lachmann, P.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.