A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand
Abstract Alpha (α)-thalassaemia is one of the most prevalent hereditary blood disorders, commonly affecting Southeast Asian people, with the highest incidence (30–40%) being seen in northern Thailand. However, this high incidence was estimated without consideration of the variations between ethnic p...
Guardado en:
Autores principales: | Mattapong Kulaphisit, Jatupol Kampuansai, Kamonlak Leecharoenkiat, Methi Wathikthinnakon, Daoroong Kangwanpong, Thongperm Munkongdee, Saovaros Svasti, Suthat Fucharoen, Duncan R. Smith, Pathrapol Lithanatudom |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/d10280ed37014a01a7f55d9243146083 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Prevalence and molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Lue ethnic group of northern Thailand
por: Suwapat Sathupak, et al.
Publicado: (2021) -
Predictive SNPs for β0-thalassemia/HbE disease severity
por: Thongperm Munkongdee, et al.
Publicado: (2021) -
Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction
por: Wasinee Kheansaard, et al.
Publicado: (2018) -
Pre-Analytical Modification of Serum miRNAs: Diagnostic Reliability of Serum miRNAs in Hemolytic Diseases
por: Yukichi Takada, et al.
Publicado: (2021) -
Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter
por: Khanita Nuamsee, et al.
Publicado: (2021)