autoimmune lymphoproliferative syndrome type 2A

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Genetics

  • associated with defects in CASP10

More general terms

References

  1. Wang J et al Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II. Cell 98:47-58, 1999 PMID: https://www.ncbi.nlm.nih.gov/pubmed/10412980

Database