Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity-Reference-Cited by-同舟云学术

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Clinical and immunological analysis of a large kindred affected by autoimmune lymphoproliferative syndrome (ALPS) due to a novel TNFRSF6 mutation displaying age dependent disease activity

Published:2022-12 Issue: Volume:245 Page:109136
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Tessarin Giulio,Baronio Manuela,Gazzurelli Luisa,Rossi Stefano,Gorio Chiara,Bertoni Elisa,Chiarini Marco,Moratto Daniele,Mazza Cinzia,Porta Fulvio,Badolato Raffalele,Lougaris Vassilios

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference8 articles.

1. Autoimmune lymphoproliferative syndrome;Oliveira;Curr. Opin. Allergy Clin. Immunol.,2004

2. Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype;Worth;Br. J. Haematol.,2006

3. The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosis;Infante;J. Pediatr.,1998

4. Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation;Magerus-Chatinet;J. Clin. Invest.,2011

5. Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome;Caminha;J. Allergy Clin. Immunol.,2010

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