APA

Fredrikson G. N., Westberg J., Kuijper E. J., Tijssen C. C., Sjöholm A. G., Uhlén M. & Truedsson L. (19961217). 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. : Journal of immunology (Baltimore, Md. : 1950).

Chicago

Fredrikson G N, Westberg J, Kuijper E J, Tijssen C C, Sjöholm A G, Uhlén M and Truedsson L. 19961217. 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. : Journal of immunology (Baltimore, Md. : 1950).

Harvard

Fredrikson G. N., Westberg J., Kuijper E. J., Tijssen C. C., Sjöholm A. G., Uhlén M. and Truedsson L. (19961217). 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. : Journal of immunology (Baltimore, Md. : 1950).

MLA

Fredrikson G N, Westberg J, Kuijper E J, Tijssen C C, Sjöholm A G, Uhlén M and Truedsson L. 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. : Journal of immunology (Baltimore, Md. : 1950). 19961217.