Asymptomatic Co-Inheritance of Hb Leiden (HBB:c.22_24delGAG), Hb Q-Thailand (HBA1:c.223G > C) and Deletional Alpha Thalassemia in a Young Chinese Male
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12288-024-01789-9.pdf
Reference5 articles.
1. De Jong WW, Went LN, Bernini LF (1968) Haemoglobin Leiden: deletion of beta-6 or 7 glutamic acid. Nature 220(5169):788–790
2. Jongbloed W, van Twillert G, Schoorl M, Schindhelm RK (2018) Unstable haemoglobin variant Hb Leiden is detected on Sysmex XN-Series analysers. Clin Chem Lab Med 56(9):e249–e250
3. Panyasai S, Satthakarn S, Pornprasert S (2018) Complex interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) disease. Hemoglobin 42(1):54–57
4. Li CG, Li CF, Li Q, Li M (2009) Thalassemia incidence and treatment in China with special reference to Shenzhen City and Guangdong province. Hemoglobin 33(5):296–303
5. Liang L, Xiao Y, Guo W, Xie T, Zheng L, Li Y (2023) Identification of double heterozygous -α4.2I/-α4.2II using third-generation sequencing. Hematology 28(1):2250646
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