Cargando…
Haemoglobinopathies in Southeast Asia
In Southeast Asia α-thalassaemia, β-thalassaemia, haemoglobin (Hb) E and Hb Constant Spring (CS) are prevalent. The abnormal genes in different combinations lead to over 60 different thalassaemia syndromes, making Southeast Asia the locality with the most complex thalassaemia genotypes. The four maj...
Autores principales: | Fucharoen, Suthat, Winichagoon, Pranee |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237250/ https://www.ncbi.nlm.nih.gov/pubmed/22089614 |
Ejemplares similares
-
Impaired Terminal Erythroid Maturation in β(0)-Thalassemia/HbE Patients with Different Clinical Severity
por: Suriyun, Thunwarat, et al.
Publicado: (2022) -
Update in Laboratory Diagnosis of Thalassemia
por: Munkongdee, Thongperm, et al.
Publicado: (2020) -
Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure
por: Wangkumhang, Pongsakorn, et al.
Publicado: (2013) -
Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis
por: Chaichompoo, Pornthip, et al.
Publicado: (2022) -
Haemoglobinopathies in tribal populations of India
por: Ghosh, Kanjaksha, et al.
Publicado: (2015)