Molecular Basis of Hereditary C1q Deficiency-Reference-Cited by-同舟云学术

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Molecular Basis of Hereditary C1q Deficiency

Published:1998-08 Issue:2 Volume:199 Page:286-294
ISSN:0171-2985
Container-title:Immunobiology
language:en
Short-container-title:Immunobiology

Author:

Petry Franz

Publisher

Elsevier BV

Subject

Hematology,Immunology,Immunology and Allergy

Reference20 articles.

1. Bacteria and complement;Petry,1998

2. Localization of the gene cluster encoding the A, B, and C chains of human C1q to 1p34.1-1p36.3;Sellar;Immunogenetics,1992

3. Characterisation and organisation of the genes encoding the A, B and C chain of human C1q;Sellar;The complete derived amino acid sequence of human C1q. Biochem. J.,1981

4. Chemistry and molecular genetics of C1q;Reid;Behring Inst. Mitt.,1989

5. Deficiency of the first component of human complement;Reid;Immunodeficiency Reviews,1989

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