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Volumn 95, Issue 11, 2006, Pages 1498-1499

Properdin deficiency in a boy with fulminant meningococcal septic shock

Author keywords

Complement; Family history; Meningococcal disease

Indexed keywords

MENINGOCOCCUS VACCINE; PENICILLIN G; POLYSACCHARIDE VACCINE; PROPERDIN;

EID: 33750408201     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1080/08035250600603008     Document Type: Article
Times cited : (13)

References (11)
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  • 7
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    • Properdin deficiency in a large Swiss family: Identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)
    • Späth PJ, Sjöholm AG, Nordin Fredrikson G, Misano G, Rohner R, Scherz R, et al. Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n). Clin Exp Immunol 1999;118:278-84.
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    • Properdin deficiency in family with fulminant meningococcal infectious
    • Sjöholm AG, Braconier JH, Söderström C. Properdin deficiency in family with fulminant meningococcal infectious. Clin Exp Immunol 1982;50:291-7.
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  • 9
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    • Inherited complement deficiency states: Implications for immunity and immunological disease
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    • Functional analysis of the classical, alternative, and MBL pathways of the complement system: Standardization and validation of a simple ELISA
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.