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Volumn 18, Issue 1, 2000, Pages 75-77

Survey of Turkish systemic lupus erythematosus patients for a particular mutation of C1Q deficiency

Author keywords

C1q deficiency; Complement deficiency; Mutation; SLE

Indexed keywords

COMPLEMENT COMPONENT C1Q;

EID: 0033975326     PISSN: 0392856X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (12)
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  • 2
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  • 3
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  • 4
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    • A homozygous point mutation results in a stop codon in the Ciq B chain of a C1q deficient individual
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  • 5
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    • Family study of natural cell activity in C1q deficient patients with systemic lupus erythematosus-like syndrome: Association between impaired natural killer cell function and C1q deficiency
    • TOTH J, STARSIA Z, BUC M, STEFANOVIC J: Family study of natural cell activity in C1q deficient patients with systemic lupus erythematosus-like syndrome: Association between impaired natural killer cell function and C1q deficiency. Immunobiol 1989: 180; 45-54.
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    • Toth, J.1    Starsia, Z.2    Buc, M.3    Stefanovic, J.4
  • 7
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    • Non-sense and mis-sense mutations in the structural genes of complement component CIqA and C chains are linked with two types of complete selective C1q deficiency
    • PETRY F, LE DT, KIRSCHFINK M, LOOS M: Non-sense and mis-sense mutations in the structural genes of complement component CIqA and C chains are linked with two types of complete selective C1q deficiency. J Immunol 1995; 155: 4734-8.
    • (1995) J Immunol , vol.155 , pp. 4734-4738
    • Petry, F.1    Le, D.T.2    Kirschfink, M.3    Loos, M.4
  • 8
    • 0029984710 scopus 로고    scopus 로고
    • Homozygous hereditary C1q deficiency and SLE: A new family and the molecular basis of C1q deficiency in three families
    • SLINGSBY JH, NORSWORTHY P, PEARCE G et al.: Homozygous hereditary C1q deficiency and SLE: A new family and the molecular basis of C1q deficiency in three families. Arthritis Rheum 1996; 39: 663-70.
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  • 9
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    • Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family
    • TOPALOGLU R, BAKKALOGLU A, SLINGSBY JH et al.: Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family. Kidney Int 1996; 50: 635-42.
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  • 10
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    • Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: Review of the cases and additional genetic and functional analysis
    • PETRY F, BERKEL AI, LOOS M: Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: Review of the cases and additional genetic and functional analysis. Hum Genet 1997; 100: 51-6.
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  • 11
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    • Dysfunctional and antigenically abnormal C1q resulting from a point mutation in codon 6 of the C chain
    • abstract
    • SUWAIRI W, BAHABRI S, BEVING D, WISNIESKI J, WARMAN M: Dysfunctional and antigenically abnormal C1q resulting from a point mutation in codon 6 of the C chain. Arthritis Rheum 40: S308 (abstract).
    • Arthritis Rheum , vol.40
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.