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J Westberg

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Journal of Clinical Immunology|August 26, 1998
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutationsG N Fredrikson, B Gullstrand, J Westberg, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
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 interchangeG N Fredrikson, J Westberg, E J Kuijper, et al.
Immunopharmacology|February 26, 1998
Human properdin deficiency has a heterogeneous genetic backgroundL Truedsson, J Westberg, G N Fredrikson, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Journal of Clinical Immunology|August 26, 1998
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutationsG N Fredrikson, B Gullstrand, J Westberg, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
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 interchangeG N Fredrikson, J Westberg, E J Kuijper, et al.
Immunopharmacology|February 26, 1998
Human properdin deficiency has a heterogeneous genetic backgroundL Truedsson, J Westberg, G N Fredrikson, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
Pageof 3