A complement C5 gene mutation, c.754G&gt;A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases

Owen, EP; Würzner, R; Leisegang, F; Rizkallah, P; Whitelaw, A; Simpson, J; Thomas, AD; Harris, CL; Giles, JL; Hellerud, BC; Mollnes, TE; Morgan, BP; Potter, PC; Orren, A

doi:10.1016/j.molimm.2014.11.010

A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases

Lookup NU author(s): Professor Claire Harris

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Author(s): Owen EP, Würzner R, Leisegang F, Rizkallah P, Whitelaw A, Simpson J, Thomas AD, Harris CL, Giles JL, Hellerud BC, Mollnes TE, Morgan BP, Potter PC, Orren A

Publication type: Article

Publication status: Published

Journal: Molecular Immunology

Year: 2015

Volume: 64

Issue: 1

Pages: 170-176

Print publication date: 01/03/2015

Online publication date: 19/12/2014

Acceptance date: 11/11/2014

ISSN (print): 0161-5890

ISSN (electronic): 1872-9142

Publisher: Pergamon Press

URL: http://dx.doi.org/10.1016/j.molimm.2014.11.010

DOI: 10.1016/j.molimm.2014.11.010

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A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases

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