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

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

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.

Affiliation

Magerus-Chatinet A; Unité INSERM 768, Hôpital Necker-Enfants Malades, Paris, France. aude.magerus@inserm.fr

J Allergy Clin Immunol ; 131(2): 486-90, 2013 Feb.

Article in En | MEDLINE | ID: mdl-22857792

Subject(s)

Autoimmune Lymphoproliferative Syndrome/genetics; Fas Ligand Protein/deficiency; Fas Ligand Protein/genetics; Mutation; Autoimmune Lymphoproliferative Syndrome/immunology; Fas Ligand Protein/immunology; Homozygote; Humans; Infant; Male

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Full text: 1 Database: MEDLINE Main subject: Fas Ligand Protein / Autoimmune Lymphoproliferative Syndrome / Mutation Limits: Humans / Infant / Male Language: En Journal: J Allergy Clin Immunol Year: 2013 Type: Article Affiliation country: France

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