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Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K. Viprakasit V, et al. Acta Haematol. 2014;131(2):88-94. doi: 10.1159/000353119. Epub 2013 Sep 26. Acta Haematol. 2014. PMID: 24081251
The origin of sickle cell disease in Thailand.
Xu JZ, Riolueang S, Glomglao W, Tachavanich K, Suksangpleng T, Ekwattanakit S, Viprakasit V. Xu JZ, et al. Among authors: viprakasit v. Int J Lab Hematol. 2019 Feb;41(1):e13-e16. doi: 10.1111/ijlh.12926. Epub 2018 Sep 27. Int J Lab Hematol. 2019. PMID: 30264513 No abstract available.
188 results