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    Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.

    Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing. gan C.A. Johnson, Peter Densen, Robert Hurford, H.R. Colten, R.A. Wetsel

    Cyhoeddwyd 1992
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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