Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome

BACKGROUND: Autoimmune lymphoproliferative syndrome (ALPS) is a rare inherited disorder characterized by defective function of Fas, autoimmune manifestations that predominantly involve blood cells, polyclonal accumulation of lymphocytes in the spleen and lymph nodes with lymphoadenomegaly and/or spl...

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Detalhes bibliográficos
Main Authors: Cerutti, Elisa, Campagnoli, Maria F, Ferretti, Massimo, Garelli, Emanuela, Crescenzio, Nicoletta, Rosolen, Angelo, Chiocchetti, Annalisa, Lenardo, Michael J, Ramenghi, Ugo, Dianzani, Umberto
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2007
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2211507/
https://ncbi.nlm.nih.gov/pubmed/17999750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2172-8-28
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