Condition: Autoimmune Lymphoproliferative Syndrome, Type IIA
rs17860403
in
CASP10
gene and
Autoimmune Lymphoproliferative Syndrome, Type IIA
PMID 10412980
1999 Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II.