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- databases for immunodeficiency-causing variations

   CASP10base
   Variation registry for  Autoimmune lymphoproliferative syndrome, type II


CASP10base mutation publications

[1999]

Search PubMed latest citations for CASP10 mutations

    1999

  • Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II.
    Wang J, Zheng L, Lobito A, Chan FK, Dale J, Sneller M, Yao X, Puck JM, Straus SE, Lenardo MJ
    Cell 1999(1): 47-58 [PubMed abstract].