Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation-Reference-Cited by-同舟云学术

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation

Published:2013-02 Issue:2 Volume:131 Page:486-490
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

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

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference22 articles.

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4. The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis;Straus;Blood,2001

5. FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function;Magerus-Chatinet;Blood,2009

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