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Hemoglobin
international journal for hemoglobin research
Volume 41, 2017 - Issue 3
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Short Communication

Hematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual

Manit NuinoonHuman Genetics Research Unit, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-1325-5489View further author information
ORCID Icon,
Nutjaree JeenduangHuman Genetics Research Unit, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand; View further author information
,
Aumpika KesornsitHuman Genetics Research Unit, School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand; View further author information
,
Dararat HorpetCenter for Scientific and Technological Equipment, Walailak University, Nakhon Si Thammarat, ThailandView further author information
&
Thunyaluk PlyduangCenter for Scientific and Technological Equipment, Walailak University, Nakhon Si Thammarat, ThailandView further author information
Pages 213-215 | Received 17 May 2017, Accepted 14 Jun 2017, Published online: 10 Aug 2017

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Hassan Abolghasemi, Sharareh Kamfar, Azita Azarkeivan, Mehran Karimi, Bijan Keikhaei, Fahimeh Abolghasemi, Mohammad H. Radfar, Peyman Eshghi & Samin Alavi. (2022) Clinical and genetic characteristics of hemoglobin H disease in Iran. Pediatric Hematology and Oncology 39:6, pages 489-499.
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Sitthichai Panyasai & Sakorn Pornprasert. (2020) Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand. Hemoglobin 44:3, pages 179-183.
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Wittaya Jomoui, Prapaporn Panichchob, Punchita Rujirachaivej, Sitthichai Panyasai & Wanicha Tepakhan. (2019) Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single Tube. Hemoglobin 43:3, pages 214-217.
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Manit Nuinoon, Orapan Thipthara & Suthat Fucharoen. (2019) Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2. Hemoglobin 43:1, pages 52-55.
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Chanchai Traivaree, Boonchai Boonyawat, Chalinee Monsereenusorn, Piya Rujkijyanont & Apichat Photia. (2018) Clinical and molecular genetic features of Hb H and AE Bart’s diseases in central Thai children. The Application of Clinical Genetics 11, pages 23-30.
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Articles from other publishers (5)

Nutjaree Jeenduang, Dararat Horpet, Thunyaluk Plyduang & Manit Nuinoon. (2024) Association of thalassemia, hemoglobinopathies, and vitamin D levels with lipid profile in adults: Community-based research in southern Thai population. Heliyon 10:10, pages e31374.
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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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Manit Nuinoon, Patchara Rattanaporn, Thongchai Benjchareonwong, Anuchit Choowet, Komsai Suwanno, Ngamta Saekoo, Krongjit Lekpetch, Orapan Thipthara, Saovaros Svasti & Suthat Fucharoen. (2022) Genetic predictions of life expectancy in southern Thai patients with β0‑thalassemia/Hb E. Biomedical Reports 16:6.
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Kritsada Singha, Goonnapa Fucharoen & Supan Fucharoen. (2021) δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia. Annals of Hematology 100:8, pages 1953-1963.
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Thanet Prajantasen, Patcharawadee Prayalaw, Sitthichai PanyasaiSukanya Binlee & Supang Nongnuan. (2021) Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand. Genetic Testing and Molecular Biomarkers 25:6, pages 426-433.
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