Article
Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran.
Hemoglobin - 1 Sept 2020
Moradi Keivan, Aznab Mozaffar, Biglari Mostafa, Shafieenia Samaneh, Azimi Azam, Bijari Nushin, Alibakhshi Reza
Abstract excerpt
Identifying couples who are carriers of thalassemia-causing mutations, followed by prenatal diagnosis (PND), is undoubtedly an effective way to prevent the birth of children with the disease. Our aim in this study was to report for the first time the spectrum of α-globin gene mutations in the population living in Hamadan Province, West Iran. Multiplex gap-polymerase chain reaction (gap-PCR), amplification...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.