A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family Acquired De Novo
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DOI: 10.1080/03630269.2019.1638797
Abstract: Abstract In Bangladesh, the practice of β-thalassemia (β-thal) carrier screening and prenatal diagnosis (PND) by β-globin gene sequencing has been initiated to prevent the birth of affected children. The study aimed to describe a novel… read more here.
Keywords: globin gene; family; hbb 27delg; novel pathogenic ... See more keywords