Authors: FREDRIKSON GN GULLSTRAND B WESTBERG J SJOHOLM AG UHLEN M TRUEDSSON L

Citation: Gn. Fredrikson et al., EXPRESSION OF PROPERDIN IN COMPLETE AND INCOMPLETE DEFICIENCY - NORMAL IN-VITRO SYNTHESIS BY MONOCYTES IN 2 CASES WITH PROPERDIN DEFICIENCYTYPE-II DUE TO DISTINCT MUTATIONS, Journal of clinical immunology, 18(4), 1998, pp. 272-282

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: TRUEDSSON L WESTBERG J FREDRIKSON GN SJOHOLM AG KUIJPER EJ FIJEN CAP SPATH PJ UHLEN M

Citation: L. Truedsson et al., HUMAN PROPERDIN DEFICIENCY HAS A HETEROGENEOUS GENETIC BACKGROUND, Immunopharmacology, 38(1-2), 1997, pp. 203-206

Authors: FREDRIKSON GN WESTBERG J KUIJPER EJ TIJSSEN CC SJOHOLM AG UHLEN M TRUEDSSON L

Citation: Gn. Fredrikson et al., MOLECULAR CHARACTERIZATION OF PROPERDIN DEFICIENCY TYPE-III - DYSFUNCTION PRODUCED BY A SINGLE-POINT MUTATION IN EXON-9 OF THE STRUCTURAL GENE CAUSING A TYROSINE TO ASPARTIC-ACID INTERCHANGE, The Journal of immunology, 157(8), 1996, pp. 3666-3671

Authors: WESTBERG J FREDRIKSON GN TRUEDSSON L SJOHOLM AG UHLEN M

Citation: J. Westberg et al., SEQUENCE-BASED ANALYSIS OF PROPERDIN DEFICIENCY - IDENTIFICATION OF POINT MUTATIONS IN 2 PHENOTYPIC FORMS OF AN X-LINKED IMMUNODEFICIENCY, Genomics, 29(1), 1995, pp. 1-8

Authors: FREDRIKSON GN TRUEDSSON L SJOHOLM AG

Citation: Gn. Fredrikson et al., NEW PROCEDURE FOR THE DETECTION OF COMPLEMENT DEFICIENCY BY ELISA - ANALYSIS OF ACTIVATION PATHWAYS AND CIRCUMVENTION OF RHEUMATOID-FACTOR INFLUENCE, Journal of immunological methods, 166(2), 1993, pp. 263-270