Associated Papers
New mutations and new phenotypes: a case of Major Histocompatibility Complex Class II Deficiency.
Li X et al.
Immunologic Research, 2024
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Mousavi Khorshidi MS et al.
Journal of Clinical Immunology, 2023
Next generation sequencing (NGS)-based approach to diagnosing Algerian patients with suspected inborn errors of immunity (IEIs).
Peng XP et al.
Clinical Immunology (orlando, Fla.), 2023
Lessons learned from the diagnostic work-up of a patient with the bare lymphocyte syndrome type II.
Damoiseaux M et al.
Clinical Immunology (orlando, Fla.), 2022
Primary immunodeficiencies in Bulgaria - achievements and challenges of the PID National Expert Center.
Naumova E et al.
Frontiers in Immunology, 2022
36211402 (PubMed )
Supplement: DataSheet_1.pdf
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency.
Suratannon N et al.
Frontiers in Immunology, 2020
32373116 (PubMed )
Supplement: Table_1.xlsx › Table_E1_Previously_diagnosed
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