CTLA4 haploinsufficiency as a predisposition to classical Hodgkin lymphoma
Author:
Affiliation:
1. Department of Pediatric Hematology Oncology and BMT, Cleveland Clinic Children’s, Cleveland, Ohio, USA;
2. Robert J. Tomsich Institute of Pathology and Laboratory Medicine, Cleveland Clinic, Cleveland, Ohio, USA
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/08880018.2019.1710310
Reference26 articles.
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3. Cutting Edge: A Soluble Form of CTLA-4 in Patients with Autoimmune Thyroid Disease
4. The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
5. CTLA-4 Gene Polymorphism at Position 49 in Exon 1 Reduces the Inhibitory Function of CTLA-4 and Contributes to the Pathogenesis of Graves’ Disease
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3. Heterozygous CTLA4 splice site mutation c.458-1G > C presenting with immunodeficiency and variable degree of immune dysregulation in three generation kindred of Caribbean descent;Pediatric Hematology and Oncology;2021-04-26
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