C5 Complement Deficiency in a Saudi Family, Molecular Characterization of Mutation and Literature Review-Reference-Cited by-同舟云学术

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C5 Complement Deficiency in a Saudi Family, Molecular Characterization of Mutation and Literature Review

Published:2013-02-01 Issue:4 Volume:33 Page:871-875
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Arnaout Rand,Al Shorbaghi Sahar,Al Dhekri Hasan,Al-Mousa Hamoud,Al Ghonaium Abdulaziz,Al Saud Bandar,Al Muhsen Saleh,Al Baik Lina,Hawwari Abbas

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/content/pdf/10.1007/s10875-013-9872-7.pdf

Reference18 articles.

1. Figueroa JE, Densen P. Infectious diseases associated with complement deficiencies. Clin Microbiol Rev. 1991;4:359–95.

2. Miller ME, Nilsson UR. A familial deficiency of the phagocytosis-enhancing activity serum related to a dysfunction of the fifth component of complement(C5) N. Engl J Med. 1970;282(7):354–35.

3. Ross SC, Densen P. Complement deficiency states and infection: epidemiology, pathogenesis and consequences of Neisserial and other infections in an immune deficiency. Med (Baltimore). 1984;63:243–73.

4. Carney DF, Haviland DL, Noack D, Wetsel RA, Vik DP, Tack BF. Structural aspects of the human C5 gene. Intron/exon organization, 5_ flanking region features, and characterization of two truncated cDNA clones. J Biol Chem. 1991;266:18786–91.

5. Ware CF, Kolb WP. Assembly of the functional membrane attack complex of human complement: formation of disulfide-linked C9 dimers. Proc Natl Acad Sci U S A. 1981;78(10):6426–30.

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