Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency
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Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency
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29
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Friday, September 1, 1995
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(Q22677535)
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"Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency" (language: en)
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J Westberg
G N Fredrikson
L Truedsson
A G Sjöholm
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