Autosomal recessive agammaglobulinemia associated with an IGLL1 gene missense mutation
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
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1. Single Mutation different Clinical Findings: IGLL1 Defect;Iranian Journal of Allergy, Asthma and Immunology;2024-08-10
2. Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia;Journal of Allergy and Clinical Immunology;2024-08
3. The assembled and annotated genome of the masked palm civet (Paguma larvata);GigaScience;2022
4. Agammaglobulinemia: from X-linked to Autosomal Forms of Disease;Clinical Reviews in Allergy & Immunology;2021-07-09
5. Update on Infections in Primary Antibody Deficiencies;Frontiers in Immunology;2021-02-11
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