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Clinical,immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review |
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| Authors: | Parisa Amirifar Mohammad Reza Ranjouri Hassan Abolhassani Tannaz Moeini Shad Amir Almasi-Hashiani Gholamreza Azizi Soraya Moamer Asghar Aghamohammadi Reza Yazdani |
| Affiliation: | 1. Department of Medical Genetics, School of Medicine, Tehran University of medical sciences, Tehran, Iran;2. Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran Contribution: Writing - original draft (equal);3. Research Center for Primary Immunodeficiencies, Iran University of medical sciences, Tehran, Iran Division of Clinical Immunology, Department of Laboratory Medicine, Karolinska Institute at Karolinska University Hospital Huddinge, Stockholm, Sweden Contribution: Writing - review & editing (equal);4. Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran Contribution: Data curation (equal);5. Department of Epidemiology, Arak University of Medical Sciences, Arak, Iran Contribution: Formal analysis (equal);6. Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran;7. School of Public Health, Student Research Committee, Hamadan University of Medical Sciences, Hamadan, Iran Contribution: Formal analysis (equal) |
| Abstract: | |
| Keywords: | familial hemophagocytic lymphohistiocytosis (FHL) Munc13-4 primary immunodeficiency diseases (PID) UNC13D |