Authors: FREDRIKSON GN GULLSTRAND B SCHNEIDER PM WITZELSCHLOMP K SJOHOLM AG ALPER CA AWDEH Z TRUEDSSON L

Citation: Gn. Fredrikson et al., CHARACTERIZATION OF NONEXPRESSED C4 GENES IN A CASE OF COMPLETE C4 DEFICIENCY - IDENTIFICATION OF A NOVEL POINT MUTATION LEADING TO A PREMATURE STOP CODON, Human immunology, 59(11), 1998, pp. 713-719

Authors: SEHNEIDER PM STRADMANNBELLINGHAUSEN B WITZELSCHLOMP K MOULDS JM BONTROP R RITTNER C

Citation: Pm. Sehneider et al., COMPARATIVE DNA-SEQUENCE ANALYSIS AND PCR SCREENING FOR THE HERV-C4 ENDOGENOUS RETROVIRAL INSERTION IN PRIMATE C4 GENES, Molecular immunology, 35(6-7), 1998, pp. 296-296

Authors: WITZELSCHLOMP K RITTNER C SCHNEIDER PM

Citation: K. Witzelschlomp et al., STRUCTURAL ORGANIZATION, DEFICIENCY MUTATIONS AND GENETIC-POLYMORPHISM OF THE HUMAN-COMPLEMENT C9 GENE, Molecular immunology, 35(6-7), 1998, pp. 298-298

Authors: WITZELSCHLOMP K HOBART MJ FERNIE BA ORREN A WURZNER R RITTNER C KAUFMANN T SCHNEIDER PM

Citation: K. Witzelschlomp et al., HETEROGENEITY IN THE GENETIC-BASIS OF HUMAN-COMPLEMENT C9 DEFICIENCY, Immunogenetics (New York), 48(2), 1998, pp. 144-147

Authors: WITZELSCHLOMP K SPATH PJ HOBART MJ FERNIE BA RITTNER C KAUFMANN T SCHNEIDER PM

Citation: K. Witzelschlomp et al., THE HUMAN-COMPLEMENT C9 GENE - IDENTIFICATION OF 2 MUTATIONS CAUSING DEFICIENCY AND REVISION OF THE GENE STRUCTURE, The Journal of immunology, 158(10), 1997, pp. 5043-5049