Another family with a silent allele of properdin factor B polymorphism (BF*QO)

[1]  H. Cleve,et al.  Properdin factor B-polymorphism , 1979, Zeitschrift für Rechtsmedizin.

[2]  K. Tokunaga,et al.  Further study on a BF silent allele , 2004, Human Genetics.

[3]  A. Ghosh.  Polymorphism of red cell glyoxalase 1 , 1977, Human Genetics.

[4]  P. Lachmann.  Inherited complement deficiencies. , 1984, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[5]  B. Olaisen,et al.  Statement on the nomenclature of human C4 allotypes. , 1983, Immunobiology.

[6]  E. Yunis,et al.  Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[7]  B. Dupont,et al.  The BF locus and HLA: rare alleles coding for functionally active and inactive factor-B products. , 1982, Human immunology.

[8]  G. Hauptmann,et al.  A hemolytically inactive gene product of factor B. , 1980, Immunobiology.

[9]  T. Strom,et al.  Improved B cell typing for HLA-DR using nylon wool column enriched B lymphocyte preparations. , 2008, Tissue antigens.

[10]  H. Cleve,et al.  Properdin factor B-polymorphism. An indication for the existence of a Bf O-allele. , 1979, Zeitschrift fur Rechtsmedizin. Journal of legal medicine.

[11]  C. Rittner,et al.  Polymorphism of the Second Component of Human Complement (C2) , 1979, Vox sanguinis.

[12]  P. Lachmann,et al.  Haemolytic diffusion plate assays for factors B and D of the alternative pathway of complement activation. , 1976, Immunochemistry.

[13]  C. Alper,et al.  GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN , 1972, The Journal of experimental medicine.

[14]  P. Terasaki,et al.  Microdroplet Assay of Human Serum Cytotoxins , 1964, Nature.