Co-inherited α-Globin Gene Cluster Duplication Compromises RBC Indices-Based Thalassemia Screening
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-022-01601-6.pdf
Reference5 articles.
1. Viprakasit V, Ekwattanakit S (2018) Clinical classification, screening and diagnosis for thalassemia. Hematol Oncol Clin N Am 32(2):193–211
2. Rund D, Rachmilewitz E (2001) Pathophysiology of alpha- and beta-thalassemia: therapeutic implications. Semin Hematol 38(4):343–359
3. Farashi S, Vakili S, Faramarzi Garous N et al (2015) Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes. Expert Rev Hematol 8(5):693–698
4. Origa R, Sollaino MC, Borgna-Pignatti C et al (2014) α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermedia. Acta Haematol 131(3):162–164
5. Liang Q, Gu W, Chen P et al (2021) A more universal approach to comprehensive analysis of thalassemia alleles (CATSA). J Mol Diagn 23(9):1195–1204
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