Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

John S. WayeHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada;Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCorrespondence[email protected]

Barry EngHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Laurie HellensHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Betty-Ann HohenadelHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Lisa M. NakamuraHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Lynda WalkerHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Citations (3)

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Jin-Mei Yan, Jian-Ying Zhou, Xing-Mei Xie, Jian Li & Dong-Zhi Li. (2016) A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]. Hemoglobin 40:3, pages 213-214.
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Articles from other publishers (2)

Amphai Phasit, Sitthichai Panyasai, Monthon Mayoon, Niphawan Jettawan & Surada Satthakarn. (2022) Phenotypic Expression of Known and Novel Hemoglobin A2-Variants, Hemoglobin A2-Mae Phrik [Delta 52(D3) Asp > Gly, HBD:c.158A > G], Associated with Hemoglobin E [Beta 26(B8) Glu > Lys, HBB:c.79G > A] in Thailand. Genes 13:6, pages 959.
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Sitthichai Panyasai, Goonnapa Fucharoen & Supan Fucharoen. (2015) Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening. Clinica Chimica Acta 438, pages 226-230.
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Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

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Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

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Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)