A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran
- 1 February 2020
- journal article
- research article
- Published by Elsevier BV in Immunology Letters
- Vol. 221, 27-32
- https://doi.org/10.1016/j.imlet.2020.01.008
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- From the Mediterranean to the Sea of Japan: The Transcontinental Odyssey of Autoinflammatory DiseasesBioMed Research International, 2013
- A Hypermorphic Missense Mutation in PLCG2, Encoding Phospholipase Cγ2, Causes a Dominantly Inherited Autoinflammatory Disease with ImmunodeficiencyAmerican Journal of Human Genetics, 2012
- SIFT web server: predicting effects of amino acid substitutions on proteinsNucleic Acids Research, 2012
- Immunology in clinic review series; focus on autoinflammatory diseases: update on monogenic autoinflammatory diseases: the role of interleukin (IL)-1 and an emerging role for cytokines beyond IL-1Clinical and Experimental Immunology, 2012
- Cold Urticaria, Immunodeficiency, and Autoimmunity Related toPLCG2DeletionsThe New England Journal of Medicine, 2012
- Mechanism of Phosphorylation-induced Activation of Phospholipase C-γ IsozymesOnline Journal of Public Health Informatics, 2010
- A method and server for predicting damaging missense mutationsNature Methods, 2010
- The role of entropy and polarity in intermolecular contacts in protein crystalsActa crystallographica. Section D, Structural biology, 2009
- Jalview Version 2—a multiple sequence alignment editor and analysis workbenchBioinformatics, 2009
- Coding of Polar and Non-polar Amino-acidsNature, 1965