Targeted resequencing of 52 bone marrow failure genes in patients with aplastic anemia reveals an increased frequency of novel variants of unknown significance only in SLX4
Author:
Publisher
Ferrata Storti Foundation (Haematologica)
Subject
Hematology
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Potential role of B- and NK-cells in the pathogenesis of pediatric aplastic anemia through deep phenotyping;Frontiers in Immunology;2024-08-20
2. Early‐life liver cirrhosis and variable clinical presentation in telomere disease;Acta Paediatrica;2022-09-13
3. The clinical and functional effects of TERT variants in myelodysplastic syndrome;Blood;2021-05-21
4. The clinical and functional effects of TERT variants in myelodysplastic syndrome;2021-02-12
5. Next‐generation sequencing in hypoplastic bone marrow failure: What difference does it make?;European Journal of Haematology;2020-10-27
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