Article
Molecular basis of HbE-beta-thalassemia and the origin of HbE in northeast Thailand: identification of one novel mutation using amplified DNA from buffy coat specimens.
Biochemical and biophysical research communications - 31 Jul 1990
Fucharoen G, Fucharoen S, Jetsrisuparb A, Fukumaki Y
Abstract excerpt
Amplification of DNA via polymerase chain reaction directly from a small amount of a buffy coat fraction was used to study the molecular basis of HbE-beta-thalassemia in the northeastern Thai population. Eight different mutations including the new one causing a beta o-thalassemia phenotype were detected. This novel mutation is an amber mutation at codon 26, which occurs at the same position as that of HbE; the...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
