Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency (Q24312024)

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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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    Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency (English)
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    J Westberg
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    G N Fredrikson
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    L Truedsson
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    A G Sjöholm
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    1 September 1995
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    29
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    1-8
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