Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency
Author:
Funder
Jeffrey Modell Foundation
Immunodeficiency Canada
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
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2. Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation;Expert Review of Clinical Immunology;2024-05-09
3. Variable Clinical Presentation of DCLRE1C Deficiency from Childhood to Adulthood;2023-10-28
4. A novel splice donor mutation in DCLRE1C caused atypical severe combined immunodeficiency in a patient with colon lymphoma: case report and literature review;Frontiers in Oncology;2023-10-12
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