Two novel CD40LG gene mutations causing X-linked hyper IgM syndrome in Vietnamese patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10238-021-00774-0.pdf
Reference21 articles.
1. Davies EG, Thrasher AJ. Update on the hyper immunoglobulin M syndromes. Br J Haematol. 2010;149:167–80.
2. Franca TT, Leite LFB, Maximo TA, et al. A novel de novo mutation in the CD40 ligand gene in a patient with a mild X-linked hyper-IgM phenotype initially diagnosed as CVID: new aspects of old diseases. Front Pediatr. 2018;6:130.
3. de la Morena MT. Clinical phenotypes of hyper-IgM syndromes. J Allergy Clin Immunol Pract. 2016;4:1023–36.
4. Winkelstein JA, Marino MC, Ochs H, et al. The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients. Medicine (Baltimore). 2003;82:373–84.
5. Leven EA, Maffucci P, Ochs H, et al. Hyper IgM syndrome: a report from the USIDNET registry. J Clin Immunol. 2016;36:490–501.
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