Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation
- 1 July 2015
- journal article
- Published by Elsevier BV in Clinical Immunology
- Vol. 159 (1), 84-92
- https://doi.org/10.1016/j.clim.2015.04.007
Abstract
No abstract availableKeywords
Funding Information
- German Federal Ministry of Education and Research (BMBF 01EO1303)
- Joint Research Fund of the Hebrew University and the Hadassah Hebrew University Hospitals
This publication has 20 references indexed in Scilit:
- Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>ALeukemia, 2013
- Gene hunting in the genomic era: Approaches to diagnostic dilemmas in patients with primary immunodeficienciesJournal of Allergy and Clinical Immunology, 2013
- The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancyBlood, 2013
- Next‐generation‐sequencing‐based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemiaGenes, Chromosomes and Cancer, 2013
- LRBA gene deletion in a patient presenting with autoimmunity without hypogammaglobulinemiaJournal of Allergy and Clinical Immunology, 2012
- LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiencyJournal of Allergy and Clinical Immunology, 2012
- Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and AutoimmunityAmerican Journal of Human Genetics, 2012
- Hereditary sensory autonomic neuropathy caused by a mutation in dystoninAnnals of Neurology, 2012
- Advances in autoimmune lymphoproliferative syndromesEuropean Journal of Haematology, 2011
- Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International WorkshopBlood, 2010