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Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation
BACKGROUND: Autoimmune lymphoproliferative syndrome (ALPS) is characterized by chronic nonmalignant lymphoproliferation, accumulation of double-negative T cells, hypergammaglobulinemia G and A, and autoimmune cytopenia. OBJECTIVES: Although mostly associated with FAS mutations, different genetic def...
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| Main Authors: | , , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2012
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| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3824280/ https://ncbi.nlm.nih.gov/pubmed/22857792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2012.06.011 |
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