C6base mutation publications [1998] [1996] [1995] [1992] Search PubMed latest citations for C6 mutations 1998 The molecular basis of C6 deficiency in the western Cape, South Africa. Hobart MJ, Fernie BA, Fijen KA, Orren A Hum Genet 1998(4): 506-12 [PubMed abstract]. Molecular defects leading to human complement component C6 deficiency in an African-American family. Zhu ZB, Totemchokchyakarn K, Atkinson TP, Volanakis JE Clin Exp Immunol 1998(1): 91-6 [PubMed abstract]. 1996 Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies. Fernie BA, Würzner R, Orren A, Morgan BP, Potter PC, Platonov AE, Vershinina IV, Shipulin GA, Lachmann PJ, Hobart MJ J Immunol 1996(8): 3648-57 [PubMed abstract]. Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals. Nishizaka H, Horiuchi T, Zhu ZB, Fukumori Y, Nagasawa K, Hayashi K, Krumdieck R, Cobbs CG, Higuchi M, Yasunaga S, Niho Y, Volanakis JE J Immunol 1996(6): 2309-15 [PubMed abstract]. 1995 Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6. Würzner R, Hobart MJ, Fernie BA, Mewar D, Potter PC, Orren A, Lachmann PJ J Clin Invest 1995(4): 1877-83 [PubMed abstract]. 1992 Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency. Orren A, Würzner R, Potter PC, Fernie BA, Coetzee S, Morgan BP, Lachmann PJ Immunology 1992(1): 10-6 [PubMed abstract].