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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Detalhes bibliográficos
Main Authors: Magerus-Chatinet, Aude, Stolzenberg, Marie-Claude, Lanzarotti, Nina, Neven, Bénédicte, Daussy, Cécile, Picard, Capucine, Neveux, Nathalie, Desai, Mukesh, Rao, Meghana, Ghosh, Kanjaksha, Madkaikar, Manisha, Fischer, Alain, Rieux-Laucat, Frédéric
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha: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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