Molecular Characterization of Hb H and AEBart’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.
Boonchai BoonyawatApichat PhotiaChalinee MonsereenusornPiya RujkijyanontChanchai TraivareePublished in: Journal of the Medical Association of Thailand = Chotmaihet thangphaet (2019)
All of the α-thalassemia mutation in our pediatric patients with Hb H and AEBart’s diseases have been characterized by the combination of molecular techniques including multiplex gap-PCR, multiplex-ARMS and DNA sequencing of HBA1 and HBA2 genes.