Interactions of electrophoretically silent hemoglobin Hekinan II [HBA1:c.84G>T] with various forms of α-thalassemias and other hemoglobinopathies: novel insights into the molecular and hematological characteristics and genetic origins

Interactions of electrophoretically silent hemoglobin Hekinan II [HBA1:c.84G>T] with various forms of α-thalassemias and other hemoglobinopathies: novel insights into the molecular and hematological characteristics and genetic origins

To determine the molecular basis, genotype – phenotype relationship, and genetic origin of Hemoglobin (Hb) Hekinan associated with several forms of α-thalassemia and other hemoglobinopathies for a better understanding of its diverse clinical phenotypes. Seventeen participants with suspected abnormal...

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Bibliographic Details
Main Authors: Sitthichai Panyasai, Prasert Chantanaskulwong, Nopphadol Permsripong, Thippawal Mokmued
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Libyan Journal of Medicine
Subjects:
Hemoglobin hekinan II
α-hemoglobin variant
α-globin haplotype
high-performance liquid chromatography
capillary electrophoresis
Online Access:https://www.tandfonline.com/doi/10.1080/19932820.2024.2406620
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https://www.tandfonline.com/doi/10.1080/19932820.2024.2406620

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