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Novel LRF/ZBTB7A variants and known HbF-modulating SNPs in transfusion-dependent β-thalassemia

Abstract Background β-Thalassemia is a hereditary blood disorder with a highly variable clinical presentation that is partly influenced by genetic modifiers that regulate fetal hemoglobin levels. Elevated HbF can ameliorate the clinical symptoms of β-thalassemia, making the identification of HbF-mod...

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主要な著者: Yunus Arikan, Tugba Karaman Mercan, Merve Embel, Erdal Kurtoglu
フォーマット: Artigo
言語:Inglês
出版事項: BMC 2025-12-01
シリーズ:BMC Medical Genomics
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オンライン・アクセス:https://doi.org/10.1186/s12920-025-02275-5
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