Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman
Author:
Affiliation:
1. Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Thailand;
2. Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand
Funder
University of Phayao
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1338185
Reference12 articles.
1. Prevalence of β-Thalassemia and Hemoglobin E in Two Migrant Populations of Manipur, North East India
2. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
3. The α-Thalassemias
4. Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis
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1. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand;Hemoglobin;2020-07-03
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