Molecular investigations on T cell subsets in patients affected by hypomorphic <i>DCLRE1C</i> mutation-Reference-Cited by-同舟云学术

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Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation

Published:2024-05-09 Issue: Volume: Page:1-7
ISSN:1744-666X
Container-title:Expert Review of Clinical Immunology
language:en
Short-container-title:Expert Review of Clinical Immunology

Author:

Karaselek Mehmet Ali¹^ORCID,Duran Tugce²,Kuccukturk Serkan³,Hazar Esra⁴,Dogar Oznur¹,Kıykım Ayca⁴,Guner Sukru¹,Reisli Ismail¹,Keles Sevgi¹⁵

Affiliation:

1. Medicine Faculty, Department of Immunology and Allergy, Necmettin Erbakan University, Konya, Turkey

2. Department of Medical Genetic, KTO Karatay University, Konya, Turkey

3. Medicine Faculty, Department of Medical Biology, Karamanoğlu Mehmetbey University, Karaman, Turkey

4. Education and Research Hospital, Department of Pediatric Immunology and Allergy, Alanya Alaaddin Keykubat University, Antalya, Turkey

5. Cerrahpasa Medicine Faculty, Department of Immunology and Allergy, Istanbul University, Istanbul, Turkey

Funder

ecmettin Erbakan University Scientific Research Projects

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/1744666X.2024.2352479

Reference29 articles.

1. Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

2. Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency

3. Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis

4. Chronic Inflammatory Bowel Disease as Key Manifestation of Atypical ARTEMIS Deficiency

5. DCLRE1C(ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

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