Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub‐Saharan Africa: implications for the susceptibility to meningococcal disease von Franco‐Jarava, C., Comas, D., Orren, A., Hernández‐González, M., Colobran, R.

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Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, Sub-Saharan Africa: Implications for the susceptibility to meningococcal disease von Franco-Jarava, Clara, Comas, David, Orren, Ann, Hernández-González, Manuel, Colobran, Roger

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Complement C5 deficiency or complement C6 deficiency found in 26% of meningococcal disease cases diagnosed in Black Africans presenting in Western Cape, South Africa von Orren, Ann, Leisegang, Felicity, Owen, Tricia, Potter, Paul, Thomas, Andrew

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Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease von Franco-Jarava, Clara, Comas, David, 1969, Orren, Ann, Hernández-González, M, Colobran, Roger

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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 case... von Owen, E. Patricia, Würzner, Reinhard, Leisegang, Felicity, Rizkallah, Pierre, Whitelaw, Andrew, Simpson, John, Thomas, Andrew D., Harris, Claire L., Giles, Joanna L., Hellerud, Bernt C., Mollnes, Tom E., Morgan, B. Paul, Potter, Paul C., Orren, Ann

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Genetic defects leading to complete deficiency of C6 occur with high frequency in South Africa von Tricia, Owen, Howard, Henderson, Paul, Morgan B., Ann, Orren

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Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family von Parham, Kelly L., Roberts, Andrew, Thomas, Andrew, Würzner, Reinhard, Henderson, Howard E., Potter, Paul C., Morgan, B. Paul, Orren, Ann

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Complement component C6 deficiency and susceptibility to Neisseria meningitidis infections : clinical practice : SAMJ forum von Orren, Ann, Potter, Paul C.

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MBL serum levels and MBL2 genotypes in South African patients with complete complement C6 deficiency (C6Q0) with or without a history of Neisseria meningitidis infections von Orren, Ann, Thomas, Andrew D., Prescott, Ruth, Potter, Paul C., Morgan, B. Paul, Garred, Peter

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Deficiency of the fifth component of complement in a young South African woman; three putative genetic defects von Owen, Elizabeth P., Edwards, Clare, Thomas, Andrew D., Henderson, Howard E., Morgan, B. Paul, Orren, Ann

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Complement component C6 deficiency and susceptibility to Neisseria meningitidis infections von Orren, Ann, Potter, Paul C

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How do mammals distinguish between pathogens and non-self? von Orren, Ann

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An abnormal but functionally active complement component c9 protein found in an irish family with subtotal c9 deficiency von Orren, Ann, O'Hara, Ann M, Morgan, B. Paul, Moran, Anthony P, Wurzner, Reinhard

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An abnormal but functionally active complement component C9 protein found in an Irish family with subtotal C9 deficiency von Orren, Ann, O'Hara, Ann M., Morgan, B. Paul, Moran, Anthony P., Würzner, Reinhard

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The molecular basis of C6 deficiency in the western Cape, South Africa von HOBART, M. J, FERNIE, B. A, FIJEN, K. A. P. M. J, ORREN, A

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Molecular bases of C7 deficiency: three different defects von Fernie, BA, Orren, A, Sheehan, G, Schlesinger, M, Hobart, MJ

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Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6 von Würzner, R, Hobart, M J, Fernie, B A, Mewar, D, Potter, P C, Orren, A, Lachmann, P J

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Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies von Fernie, BA, Wurzner, R, Orren, A, Morgan, BP, Potter, PC, Platonov, AE, Vershinina, IV, Shipulin, GA, Lachmann, PJ, Hobart, MJ

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Heterogeneity in the genetic basis of human complement C9 deficiency von Witzel-Schlömp, K, Hobart, M J, Fernie, B A, Orren, A, Würzner, R, Rittner, C, Kaufmann, T, Schneider, P M

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Hepatic and extrahepatic microsomal electron transport components and mixed-function oxygenases in the marine fish stenotomus versicolor von Stegeman, John J., Binder, Robert L., Orren, Ann

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