Molecular Characterization of Hb H and AEBart ’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.

Conclusion: 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. PMID: 29916623 [PubMed - in process]

https://www.ncbi.nlm.nih.gov/pubmed/29916623?dopt=Abstract

Source: Journal of the Medical Association of Thailand = Chotmaihet thangphaet - June 21, 2018 Category: General Medicine Tags: J Med Assoc Thai Source Type: research